Baxter Healthcare Corporation recalls APD Drain Manifold
Recalled Product
APD Drain Manifold
Hazard / Issue
Certain Peritoneal Dialysis product codes do not have FDA regulatory clearance and were distributed within the United States in error.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Product code: R5C4512; UDI: 00085412008790; Lot Number: H18D03030 (exp. date: 04/03/2023), Lot Number: H18E31046 (exp. date: 05/31/2023), Lot Number: H18L04065 (exp. date:12/04/2023), Lot Number: H20H10073 (exp. date: 08/10/2022)
View official government recall
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