Procedure packs contained a recalled product.
Reason for recall: Procedure packs contained a recalled product. Distribution: US Nationwide distribution in the states of OH and TN. Quantity: 1306 kits Lot/code info: NS CVR PREP PACK /89-6817.09; Lots 56391514 (exp 08/01/2023), 56926777 (exp 08/01/2023), 57103035 (exp. 08/01/2023); UDI-DI (GTIN): 00749756730938 NON-STERILE IR ADMISSION KIT / 89-8762.05; Lot 57104020 (exp 07/01/2023); UDI-DI (GTIN): 00749756883627
00749756730938, 00749756883627
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.