FDA Device recall Z-1945-2014
Baxter, MiniCap with Povidone-Iodine solution, 5C4466P. For dialysis
- FDA Device
- Class II
- terminated
- Published 2014-07-09
On 2014-07-09 the FDA classified a Class II recall of Baxter, MiniCap with Povidone-Iodine solution, 5C4466P. For dialysis by Baxter Healthcare, citing 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 ove….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1945-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-07-08 |
| Published | 2014-07-09 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Baxter Healthcare |
| Distribution | AL, AR, KS, MO, MS, TN, TX |
Product
Baxter, MiniCap with Povidone-Iodine solution, 5C4466P. For dialysis.
Reason
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.
Identifiers
| code_info | Lot Numbers: GD894535, GD894550 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1945-2014%22
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