Abstract: Absorbent articles incorporating a wetness sensor for indicating the presence of a body fluid are disclosed. In particular, the absorbent articles include at least two conductive elements that form an open circuit within the article. Each conductive element is connected to a conductive pad member that has sufficient surface area in order to facilitate connection to a signaling device. In accordance with the present disclosure, various attachment mechanisms are disclosed for attaching the pad members to a signaling device. In particular, although the absorbent articles are disposable, the signaling device is intended to be used with multiple absorbent articles. Therefore, a simple and efficient method of connecting the signaling device to the pad members provides various advantages. In one particular embodiment, for instance, the pad members comprise a conductive loop-type material that is attached to a corresponding conductive hook-type material on the signaling device.

Abstract: An improved method for measuring and automatically disposing of infectious waste generated during and after surgical and clinical procedures is provided. The infectious waste removal device includes a suction source, a method for pressure verification, separation chamber for isolating fluids, containment reservoir, measurement chamber for determining fluid received, an information source for such fluid volumes, a quantitative method for calculating fluid dynamics, a post use cleaning method, and other attributes for use by the surgical team or healthcare staff in order to while minimize healthcare worker handling of said infectious waste and to limit their possible exposure.

Abstract: A suction fluid collector includes a transparent reservoir made of a resilient material with an upper opening positioned on one side of a flexible suction bag with at least one transparent side. A plate part made of a resilient material is positioned on another side of the suction bag opposite said reservoir. An urging means arranged between the reservoir and the plate part provides a force tending to expand a gap between the reservoir and the plate part. A suction tube is positioned partially inside the reservoir and extends through the suction bag.

Abstract: A weight scale including: a measuring electronic circuit including a filter; a load cell attachable to a support housing and generating a load signal processed by the filter of the electronic circuit; a spring coupled to the load cell to apply a force to the load cell, wherein the load signal is indicative of the force, and a scale beam connected to the spring and to the support housing, wherein a weight to be measured is attached to the scale beam and the force applied by the spring is indicative of the weight, and wherein natural frequencies of the weight and spring is higher than a cut-off frequency of the filter.

Abstract: A collection system for collecting, testing and transporting liquid biological specimens that limits exposure of a tester to the liquid sample and keeps the collected samples pristine even after exposing some of the sample to test strips. The system includes a collection body for receiving and holding a liquid sample, a lid that is coupled to the body, and a test strip housing. The lid includes a transfer conduit while the test strip housing includes an opening defined within the test strip housing. The transfer conduit and the opening are aligned when the test strip housing is coupled to the lid. When the system is moved or tilted, some of the liquid sample moves through the transfer conduit and the opening into the test strip housing.

Abstract: An open circuit gravity-assisted uroflowmeter has a urine collector having a generally open inlet in fluid communication with a sensing passage located at a lower elevation than the inlet, the sensing passage intersecting a magnetic field and having electrodes for detecting a flow-dependent voltage induced by the passage of urine through the magnetic field. Preferred embodiments of the uroflowmeter may have low pressure drop, rapid response and simple construction.

Abstract: A skin penetrating system includes a housing member and a penetrating member positioned in the housing member. An analyte detecting member is coupled to a sample chamber. The analyte detecting member is configured to determine a concentration of an analyte in a body fluid using a sample of less than 1 ?L of a body fluid disposed in the sample chamber. A tip of the penetrating member is configured to extend through an opening of the sample chamber.

Abstract: Absorbent articles incorporating a wetness sensor for indicating the presence of a body fluid are disclosed. In particular, the absorbent articles include at least two conductive elements that form an open circuit within the article. Each conductive element is connected to a conductive pad member that has sufficient surface area in order to facilitate connection to a signaling device. In accordance with the present disclosure, various attachment mechanisms are disclosed for attaching the pad members to a signaling device. In particular, although the absorbent articles are disposable, the signaling device is intended to be used with multiple absorbent articles. Therefore, a simple and efficient method of connecting the signaling device to the pad members provides various advantages. In one particular embodiment, for instance, the pad members comprise a conductive loop-type material that is attached to a corresponding conductive hook-type material on the signaling device.

Abstract: Embodiments of the present invention provide an apparatus and method controlling the flow of aspiration fluid in an aspiration chamber of a surgical cassette. One embodiment of the present invention provides an aspiration chamber having an aspiration port positioned at or close to the bottom of the chamber. When the aspiration fluid enters the aspiration chamber from below the fluid surface (e.g., from a port located at the bottom or on a sidewall close to the bottom), it does not create disturbance at the liquid/air interface and thus does not disturb the continuous level sensing. Also, since the aspiration port is placed at or very close to the bottom of the aspiration chamber, the liquid inside the chamber can be fully used for sustained reflux and push priming.

Abstract: A lateral flow assay device for testing a bodily fluid, such as urine, blood, mucous, saliva, etc., is provided. The lateral flow assay device includes a chromatographic medium (e.g., porous membrane) that defines a detection zone that provides a signal indicative of the presence or amount of bilirubin or urobilinogen. The device may also include a control zone that provides a signal indicative of whether a sufficient amount of bodily fluid has been provided and tested. In one embodiment, the device is integrated into an absorbent article to provide a user or caregiver with rapid information about a health condition. For example, the device may be integrated into a diaper to provide information about the presence of bilirubin and/or urobilinogen. This information may provide an early warning system to allow the user or caregiver to seek additional testing and/or treatment. Alternatively, semi-quantitative or quantitative results may be derived from the test.

Abstract: To allow a DC voltage to be obtained as an output signal for higher versatility. A sensor unit 400 has three electrodes: a transmission electrode 401, a reception electrode 402 and a shielding electrode 403. The shielding electrode 403 shields the transmission electrode 401 and the reception electrode 402 from each other in terms of high-frequency and is constantly earthed. A high-frequency voltage is applied to the transmission electrode 401 from a high-frequency oscillation circuit 410. A high-frequency voltage depending upon the magnitude of the electrostatic capacity between the electrodes 401 and 4023 is outputted from the reception electrode 402. The high-frequency voltage outputted from the reception electrode 402 is converted into a DC voltage by a detection circuit 420. The presence or absence or the amount of a substance is determined based on the magnitude of the DC voltage produced in the detection circuit 420.

Abstract: A method is provided for measuring the insertion distance of an intravaginal article within a human vaginal cavity. The method uses a measuring device, which can be slidably attached to a withdrawal means of a vaginally inserted intravaginal article. The measuring device may be moved along the withdrawal means to a predetermined position, and then fixedly secured to the withdrawal means. The intravaginal article is then removed from the vaginal cavity and the insertion distance determined.

Abstract: A collection container for collecting biological fluid specimens having an integral fill-line indicator which corresponds to a desired specimen volume is disclosed. The integral fill-line indicator may comprise a ridge that is raised from the surface of the collection container. The integral fill-line indicator may also be altered by surface modification to impart a distinct visual appearance and/or texture. The collection container may have a single or a plurality of integral fill-line indicators which correspond to a desired specimen volume range. A method of manufacturing a collection container having an integral fill-line indicator is also disclosed.

Abstract: These and other objects of the present invention are achieved in a body fluid sampling system for use on a tissue site that includes an electrically powered drive force generator. A penetrating member is operatively coupled to the force generator. The force generator moves the member along a path out of a housing having a penetrating member exit, into the tissue site, stops in the tissue site, and withdraws out of the tissue site. An analyte detecting member is positioned to receive fluid from a wound created by the penetrating member. The detection member is configured to determine a concentration of an analyte in the fluid using a sample of less than 1 mL of the fluid.

Abstract: A body fluid sampling unit includes a puncture device including a needle having a sharp needle point and a drive mechanism for operating the needle to puncture a living body surface with the needle point, a tip including an introducing section for introducing a body fluid flowing out from a puncture portion of the living body surface punctured with the needle point, a test paper for detecting a predetermined component in the body fluid, and a tip body mounted to a component measuring device for measuring the quantity and/or property of the predetermined component detected by the test paper; and a case including a mechanism containing section for containing the puncture mechanism so that the needle point of the puncture mechanism can be moved by the drive means, and a sampling implement containing section for containing the body fluid sampling implement so that the tip can be taken out.

Abstract: An apparatus for testing a specimen. The apparatus having means for withdrawing a small sample of the specimen thereby preventing the potential contamination of the majority of the specimen.

Abstract: A system for collecting urine specimens from pet or animal comprising an elongated tray section having at one end a collection chamber for collecting a predetermined volume of urine in fluid communication with an open section of said tray to receive a stream of urine from the pet or animal, a discharge port at the opposite end of said tray and a specimen vial removably mounted to the discharge end of said tray whereby when an animal is urinating, the device is positioned under the stream with the collection chamber end downwardly inclined so that a sufficient quantity flows into the collection chamber to predetermined level and then tilting the device in a reverse direction so the collected sample flows into the specimen vial and is sealed.

Abstract: A collection device for a testing system includes a central volume and a trough, adjacent the central volume. The trough is configured with a pour spout such that, as fluid is poured from the collection device, a controlled volume remains in the trough. The trough is configured to receive a portion of a test kit and to apply the controlled volume of the sample to test strips within the test kit. The trough can also include apertures in the wall between the trough and the central volume which allow excess sample to flow back into the cup when the cup is placed upright after pouring and when the test kit is inserted into the trough.

Abstract: A surgical sponge detection system includes a plurality of surgical sponges (2) having radio frequency identification tags (1) securely attached thereto and a non-optical hand-held reader (40) for detecting the sponges by detecting the tags (1). Also disclosed is a device (30) for automatically counting, weighing, and calculating blood loss contained within, soiled surgical sponges (2) which includes a cabinet with an opening (3) at the top through which sponges (2) are deposited, a reader (6) which scans each sponge (2) entered and determines sponge type from a tag (1) affixed to each sponge (2), and a disposable bag (8) into which the sponges (2) are deposited.

Abstract: A device for accessing biological fluid, sampling biological fluid constituents and determining the concentration of at least one target constituent within the accessed biological fluid is provided. The device has at least one micro-piercing member used to penetrate the skin to a selected depth and to access biological fluid, a constituent sampling means and a constituent measuring means. The constituent sampling means comprises a constituent transfer medium, such as a hydrophilic gel material, by which sampled constituents are transferred from the micro-piercing member to the measuring means. The measuring means includes an electrochemical cell having at least one porous electrode through which at least one sampled constituent is caused to enter into the electrochemical cell. Methods of sampling constituents within the skin and measuring the sampled constituents, as well as kits for practicing the invention are provided.

Abstract: The invention relates to a urological instrument (1) for assessing a urine flow, comprising a receiving member (5) for the urine flow which, at least during operation, is in open liquid communication with a urine guide (6). The urine guide (6) leads to an inlet of flow indicator means (7) for assessing at least a magnitude of the urine flow. The receiving member (5) has a first, relatively compact storage state and a second, expanded ready-to-use state and is designed and adapted to allow it to be brought manually from the storage state to the ready-to-use state. At least in the ready-to-use state the receiving member comprises a cavity open on at least one side for receiving the urine flow therein.

Abstract: A wound irrigation kit includes a basin for collecting irrigation fluid that is configured to closely fit the specific body part that is to be irrigated. The kit optionally includes a grommet that can be readily incorporated into the basin to allow for active draining of the basin during the irrigation procedure. The kit also optionally includes a flexible irrigation shield that can be attached to an existing irrigation device and that can be readily modified to vary its length.

Abstract: To allow a DC voltage to be obtained as an output signal for higher versatility. A sensor unit 400 has three electrodes: a transmission electrode 401, a reception electrode 402 and a shielding electrode 403. The shielding electrode 403 shields the transmission electrode 401 and the reception electrode 402 from each other in terms of high-frequency and is constantly earthed. A high-frequency voltage is applied to the transmission electrode 401 from a high-frequency oscillation circuit 410. A high-frequency voltage depending upon the magnitude of the electrostatic capacity between the electrodes 401 and 4023 is outputted from the reception electrode 402. The high-frequency voltage outputted from the reception electrode 402 is converted into a DC voltage by a detection circuit 420. The presence or absence or the amount of a substance is determined based on the magnitude of the DC voltage produced in the detection circuit 420.

Abstract: An inexpensive and disposable, highly absorbent pad for placement on a floor surface, directly in front of a urinal, for absorbing fluid not deposited within the confines of the urinal which would otherwise drip on the floor. Fluid absorbed by the pad is prevented from reaching the underlying floor thereby eliminating the problems associated with fluids being deposited on the floor. The pad includes a normally concealed incorporates a normally concealed, flexible, thin plastic disposal container connected to a pad removal member. The disposal container is stored in a normally concealed location, preferably beneath the pad, and automatically deploys and envelops the pad when a force is exerted on the removal member during the pad removal process.

Abstract: A device for weighing fluid includes a scale from which a fluid receptacle is suspended. Oscillations in the weight reading due to the pendulous motion of the receptacle are suppressed by a digital filter selected to have rejection notches at the frequencies of weight oscillation.

Abstract: An apparatus for measuring the discharge of a liquid, in particular urine, from a patient. The apparatus includes a measuring container (1), means (H) for applying a first acoustic signal to the liquid-empty part of the measuring container (1), means (H) for recording a second acoustic signal generated in the measuring container (1) in response to the first signal, means (45) for determining a current liquid amount in the measuring container (1) on the basis of the second acoustic signal. The measuring container (1) has a measuring pipe (5) defining a liquid-empty resonance chamber for generating the second acoustic signal.

Abstract: A pH sensor for the visual or optical indication of the pH of a sample. The pH sensor includes a hydrophilic, optionally intrinsically charged or neutral, synthetic membrane and at least one pH indicator dye immobilized thereto, so as to prevent appreciated bleeding of the at least one indicator dye from the synthetic membrane upon immersion in an aqueous liquid.

Abstract: A kit includes all the materials necessary for oral gastric lavage in a single pouch. The components, many of which are common hospital supplies, may thus be pre-selected to work together in critical applications and to resist clogging.

Abstract: A wound treatment apparatus is disclosed to provide vacuum therapy to a wound associated with a patient. The wound treatment apparatus comprises a control unit comprising an alarm and a display displaying an alarm log providing information associated with each activation of the alarm. The display also displays information to instruct a user how to operate the wound treatment apparatus. A method of calibrating the control unit is disclosed.

Abstract: An upright female urine collector having a horizontally accordion pleated rectangular shaped urine collection receptacle with a tube outlet, the tube housing a manually operated two way valve disposed to direct urine flow either to a sample reservoir containing a chemical reagent test strip or to a urine sample collector. The two way valve can be spring activated or can be hand turned for instant urine flow redirection. In an alternate embodiment, an upright female urine collector has a urine collection receptacle modified to retain the chemical reagent test strip in a trench with exit means for quick test results observation.

Abstract: A collection cup for a drug testing system includes a central volume and a trough, exterior to the central volume. The trough is configured with a pour spout such that, as fluid is poured from the cup, a controlled volume remains in the trough. The trough is configured to receive an on-site test kit and to apply the controlled volume of the fluid to test strips within the on-site test kit. The trough also includes two apertures in the wall between the trough and the central volume which allow excess fluid to flow back into the cup when the cup is placed upright after pouring and when the test kit is inserted into the trough.

Abstract: A method of analysis of vaginal secretions collected in an absorbent pad is disclosed. The method is effected by implementing the steps of (a) using an absorbent pad for collecting the vaginal secretions, the absorbent pad including an inner membrane for absorbing at least a portion of the secretion, the inner membrane being embedded among layers of the absorbent pad, and an external, viewable membrane including a color indicator for indicating a location of secretions absorbed by the absorbent pad according to at least one parameter being indicative of a pathological state; and (b) if the pathological state is indicated, biochemically analyzing the inner membrane at a location respective to the location of secretions absorbed by the absorbent pad for further characterizing the pathological state.

Abstract: A device for collecting urine includes a container kept at vacuum, an interface locatable at the urethral opening of a person and a pump operable to create a vacuum within the container. A sensor senses the presence of urine at the interface and opens a valve to allow the pumping of urine from the interface to the container.

Abstract: A urine cup carry-in apparatus according to the present invention includes a casing set close to a urine cup carrying line, a carry-in mechanism set inside the casing and including a urine cup holder which holds a urine cup, the urine cup holder being movably provided such that the urine cup is allowed to be automatically carried into the urine cup carrying line, and an information message display device and a voice guide device arranged adjacent to each other to present an operation guide to an operator including at least means for setting a urine cup containing urine into the urine cup holder and means for starting a carry-in operation of the urine cup holder which holds the urine cup.

Abstract: An improved drainage apparatus for use in pleural aspiration of patients during thoracic surgery. The Apparatus includes three tubes mounted in parallel and connected to one another. A first tube acts as a vacuum input tube; the second tube is a flow monitor tube, while the third tube is filled with water and keeps the vacuum system isolated from the atmosphere.

Abstract: A urine collection cup device is provided including a clear plastic cup, a reagent strip disposed against an inner surface of the cup and adhered thereto by means of a plastic laminate or adhesive member. An aperture is provided in the adhesive member on a sample introduction end of the reagent strip to enable a fluid sample to be introduced onto the reagent strip. By capillary action the fluid migrates up the reagent strip and causes a visible indication of test validity and test results. A second aperture covered with a hydrophobic material is provided adjacent the reagent strip end to enable air to vent from the strip while preventing fluid specimen from entering therein.

Abstract: A disposable thoracic drainage device connectable to an aspiration unit, comprising a container body internally forming at least one chamber for collecting the drainage liquid which is connected to an inlet for connection to a patient and to a water-head suction adjustment valve. The water-head suction adjustment valve has a first water head section and a second water head section which are side by side and mutually series-connected by a connecting duct.

Abstract: A single, integrated device in which a body fluid (e.g., blood) of a human or animal can be both collected and analyzed easily and without risk of contamination is disclosed. The collection portion and analysis portion of the device are permanently joined to permit movement of small quantities of body fluid under controlled conditions, to minimize any waste of the body fluid, to ensure that no contamination reaches the main body fluid volume, and to create a permanent physical record of the results of the analysis in association with the fluid sample itself: A wide variety of different body fluid components which may be indicative of various diseases, dysfunctions and abnormalities of the human or animal or the body fluid itself can be tested for.

Abstract: A container for examination and storage of a placenta includes a bottom wall, at least one substantially upright side wall joined to the bottom wall to define an interior and an open top. The side walls and/or the bottom wall have indicia thereon adapted to measure the size of the placenta in three dimensions. Indicia are also provided to measure the umbilical cord. The container is stackable for storage, and labeling areas are provided. A basic method of examining a placenta is disclosed, along with further steps and variations.

Abstract: A fluid recovery system, such as a chest or thoracic cavity drain, having a collection chamber for collecting fluid from a patient includes a base and a front face having a translucent portion for viewing the collected fluid and monitoring operation of the system. The front face is coupled to the base at an acute angle to facilitate viewing of the collected fluid, and measurement of the fluid volume, from a position substantially above the fluid recovery system. Additionally, a column insert can be positioned within the collection chamber to collect an initial volume of the fluid and to allow precise determination of its volume.

Abstract: A combination receptacle and fluid immobilizer is disclosed for collecting a fluid. The receptacle has a bottom and sidewalls joined to the bottom to form at least a partially enclosed void area. The receptacle has an opening through which a fluid can be collected and later removed. A flushable, fluid immobilizer is positioned within the receptacle and is absorbent. The fluid immobilizer is formed from a multitude of randomly oriented cellulosic fibers that are elastically stressed and bonded by only hydrogen bonds. The fluid immobilizer is capable of capturing and immobilizing fluid which is collected in the receptacle such that the fluid can be transported to a discharge location without having to worry about spillage.

Abstract: A computer based system for tracking a patient's fluid volume and electrolyte (cation or anion concentration) balances, during the period extending from before surgical procedures through the recovery process, which will assist the attending physician in maintaining proper balances in the patient. The system contains automatic sensors for measuring the volumes of fluids administered to and recovered from the patient. The system also preferably contains sensors for measuring electrolyte concentrations in these fluids, and, when sensors are not available, assists the attending physician in estimating. The system assists the attending physician in creating baseline values for a patient's fluid and electrolyte values, and then accounts for the fluids going into and out of the patient to continuously track current values. Out of bounds conditions for these balances, when detected, will cause the system to issue alarms and make suggestions to the attending physician for remedial action.

Abstract: A waste liquid collection system for use in continuous arteriovenous or venovenous hemodialysis (CAVH or CVVH) is disclosed. The system comprises a collection vessel and associated interconnection lines which can be preset to given volume of waste liquid to be removed from the dialysis machine in a given period of time. Once the volume is reached, the collection vessel stops waste liquid flow until the vessel is emptied and reset. The system guaranties that excess liquid will not be removed from a patient.

Abstract: A removable lid (10) for an analytical specimen cup (12) of a type for defining a test space (26) with a chemical strip (24) mounted therein includes a selectively-removable protective cover (16) for selectively covering and uncovering an outer surface of a transparent portion of an outer partition (18) forming the test space. The protective cover is formed as one piece with an inner partition to be attached thereto by a dual living hinge (28a and b). The lid is rectangular in shape and includes an elongated magnifying lens (20) which has protrusions extending into blind holes (62) of the inner partition. The magnifying lens extends across the transparent portion of the outer partition. When the protective cover is in a closed position it impinges on the magnifying lens. A peel-off color analysis chart (22) is mounted on an inside surface of the protective cover.

Abstract: Disposable paper products, such as paper toweling, are provided with an indicator means which is disposed on said disposable paper product in a discontinuous or combination discontinuous/continuous pattern. The indicator means gives a visually recognizable signal to a user that desirable properties of the disposable paper product are maintained, even after the disposable paper product has become wetted with a substantially transparent aqueous liquid. The wet gray scale difference for the disposable paper product of the present invention is at least about 64 gray scale units when the disposable paper product is wetted with a substantially transparent aqueous liquid.

Abstract: A monitor is disclosed for measuring a liquid discharged from a patient's body. A housing defines a cavity having a floor. A substantially rigid wall container is removably positioned within the cavity, the container having a bottom wall portion supported on the floor of the cavity. A transducer is mounted in the floor of the cavity and engages the bottom wall portion of the container. The transducer is periodically engaged to transmit energy through the bottom wall portion and into a pool. The time duration required for the transmitted energy to travel from the transducer means to the upper surface of the pool and back again is determined, and this time duration is converted into a volume of fluid by reference to a look-up table, a mathematical algorithm, or both. The monitor includes an optical sensor to detect the presence of a container in the housing and provides an indication if no container is detected.

Abstract: A device 10 detects the presence of occult blood in feces by employing a sheet 12 of brittle material in which are formed a plurality of chambers 18 holding a liquid reagent solution juxtaposed to an absorbant material 14 impregnated with a guaiac material. The individual chambers 18 provide individual liquid tight enclosures that have thin walls that rupture to release the reagent solution when the device 10 is used to wipe feces from the rectum. The reagent solution reacts with the guaiac material to produce a blue color in the presence of occult blood in the feces.

Abstract: A device for collecting uncontaminated liquid specimens, particularly, urine specimens from adult females, adult males and pediatric males. The device includes an elongated flexible tubular conduit member having a funnel-shaped opening at one end to be in sealing relationship with a urethra or glans penis and a discharge end to be received within a sample container. The sample container includes an opening with a sealing member therein to receive the discharge end of the elongated flexible tubular conduit member in an open position for receiving a urine specimen therein and in a closed position when the discharge end of the elongated flexible tubular conduit member is withdrawn.

Abstract: An apparatus for minimizing trauma to a medical fluid while transporting the medical fluid from a surgical wound by reducing the air to fluid interface during transport. The apparatus includes a suction wand for collecting medical fluid and tubing for transporting the medical fluid to a reservoir. The reservoir repeatedly accumulates the medical fluid and discharges it in a bolus when a predetermined volume is achieved. The reservoir comprises a fluid inlet, a fluid outlet, and a gas outlet. A siphon is disposed inside the reservoir for removing the bolus of medical fluid once the predetermined fluid volume is accumulated. The siphon includes a first end for suctioning the medical fluid and a second end exiting the reservoir through the fluid outlet, thereby defining an external siphon length. A pump is attached to the second siphon end to provide suction to the system.

Abstract: A cassette for collection of fluids in a fluid aspirating system which may be reusable after sterilization. The cassette includes vacuum aperture and an aspiration port along the top wall of the cassette. Aspiration tubing is connected to the aspiration port at one end and is seated within an upstanding retainer at the proximal edge of the top wall at the opposite end. Internally, the cassette includes structures to increase flow impedance so that liquid is not drawn into the vacuum port when the fluid level rises. In addition, a pivot mechanism is disposed about a pivot hub within the chamber. A float is disposed on the pivot mechanism at a radius from the pivot hub for intercepting the vacuum port as aspirated fluid fills the chamber. As the fluid level rises, a light path is intercepted by the float to terminate aspiration. However, the float also mates with the vacuum port to close off the flow path. Thus, the system prevents overfilling of the container if the optical detector fails.