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.
Reason for recall: 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. Distribution: US nationwide distribution, and Canada. Quantity: 162 units Lot/code info: UDI/DI (case) M7524111UTI0, UDI/DI (kit)M7524111UTI0, Serial/Lot Numbers: 22229491074
22229491074
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.