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The potential for cracks forming in the breathing circuit hose.
Due to manufacturing issues there is a potential for the catheter sheath to detach.
Identified faulty cartridges. If such a faulty cartridge is used for sample testing, false test results could occur.
Catheters indicated for short-or-long term access to the central venous system have tubing that exceeded melt flow index specification (higher), which could lead to increased material fatigue leaks, which could lead to infiltration, extravasation, discomfort, phlebitis, bleeding, air embolism, foreign body embolism, infection and interruption to therapy.
Incorrect software flagging may occur for the assay that may potentially lead to an erroneous result.
Due to a software bug, automated dispensing cabinet is unable to calculate countback discrepancies during the issue process, which causes incorrect transaction quantity to be recorded. This bug can also result in the CUBIE opening more times than needed for the transaction to be completed, which may result in a patient receiving more than the intended dose of medication.
Users trying to restock a single bin location of an automated dispensing cabinet, during pocket exchange restocking workflow, may experience a software issue that results in 2 destock transactions and 2 stock transactions, which results in doubling the bin quantity, which may result in a delay in access to desired medications and/or supplies, which may lead to temporary body function impairment.
Due to a software issue, when attempting to restock the automated dispensing cabinet, user have received the banner message "Stocking window has passed, or item has been removed from purchase order. Please contact Pharmacy for assistance". When this occurs, the medication cannot be restocked and can potentially lead to delays in accessing medication for patients.
Incorrect resistor utilized in the VH-3010 Power Supply, which may cause the Jaws of the HemoPro 2 to not adequately head up.
Potential for collimator to fall as a result of incorrect installation.
Nerve Monitoring System with certain software versions has potential for increased stimulus artifact, which may require troubleshooting, and may lead to procedure delay, extubation, and medical intervention.
The devices are missing the laser marked depth markings.
Identified curing issues with the silicone during the needles manufacturing process.
The incorrect value of the International Sensitivity Index (ISI) is printed on the outer box label.
The battery for certain ultrasound systems can potentially develop an internal failure which could result in smoke or fire.