Baxter — Class II medical device recall Z-1945-2014
Terminated recall by Baxter Healthcare Corp., reported 2014-07-09, distributed in AL, AR, KS, MO, MS, TN, TX. the white printed paper layer on the pouch packaging may not be fully adhered to the pouch foil layer. The upp
| Recall number | Z-1945-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corp., Deerfield, IL, United States |
| Recall initiated | 2013-07-08 |
| Classified | 2014-06-30 |
| Reported by FDA | 2014-07-09 |
| Terminated | 2014-06-30 |
| Distributed | AL, AR, KS, MO, MS, TN, TX |
| Quantity | 20,940 units |
| Lot numbers | GD894535, GD894550 |
Product
Baxter, MiniCap with Povidone-Iodine solution, 5C4466P. For dialysis.
Reason for recall
the white printed paper layer on the pouch packaging may not be fully adhered to the pouch foil layer. The upper paper layer may serve as a protective barrier and help support overall packaging.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1945-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.