Reported Apr 6, 2022 · Terminated
MiniCap Extended Life PD Transfer Set Product Codes: 5C4482S, R5C4482, R5C4483, R5C4484
Baxter Healthcare Corporation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Baxter Healthcare Corporation · 1 Baxter Pkwy · Deerfield, IL · 60015-4625
Is this the product you have?
- MiniCap Extended
- Life PD Transfer Set Product Codes
5C4482SR5C4482R5C4483R5C4484
- Lot codes and dates
5 of 5 products
Products covered by this recall Model / number Barcodes Product as published 5C4482S0085412476261UDI: 0085412476261 R5C44820085412008776Lot Number (Expiration Date): H20F02074 (06/02/2025) and H21C31053 (03/31/2026) , UDI: 0085412008776 R5C44830085412008783Lot Number (Expiration Date): H18E18050 (05/18/2023), H20K06084 (11/06/2025), H20L08070 (12/08/2025), H21E07058 (05/07/2026), H21F07049 (06/07/2026), H21F08070 (06/08/2026), H21F28060 (06/28/2026), H21K16066 (11/16/2026) , UDI: 0085412008783 R5C44840085412050768Lot Number (Expiration Date): H18A12037 (01/12/2023) and H20K06035 (11/06/2025) , UDI: 0085412050768 — Lot Number (Expiration Date): H17H03057 (08/03/2022), H18G16076 (07/16/2023), H19E31052 (05/31/2024), H21B16056 (02/16/2026) - Amount recalled
- 498 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
Devices distributed lacked regulatory clearance.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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