All Recalls

Boxes contain a reduced concentration of Nicotinamide Adenine Dinucleotide and does not provide enough of the blood factors necessary to support Haemophilus growth. The reduction could cause a false negative result for Haemophilus isolation in a clinical specimen.

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Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in the sterility of the kit.

DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.

Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in the sterility of the kit.

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There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.

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Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in the sterility of the kit.

Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in the sterility of the kit.

DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.

DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.

Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in the sterility of the kit.

Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in the sterility of the kit.

DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.

There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.

Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in the sterility of the kit.