FDA Device recall Z-1565-2013
Baxter, MiniCap with Povidone-Iodine solution, 5C4466P, Baxter Healthcare Corporation
- FDA Device
- Class II
- terminated
- Published 2013-07-03
On 2013-07-03 the FDA classified a Class II recall of Baxter, MiniCap with Povidone-Iodine solution, 5C4466P, Baxter Healthcare Corporation by Baxter Healthcare, citing leaking pouches.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1565-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-05-21 |
| Published | 2013-07-03 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
Product
Baxter, MiniCap with Povidone-Iodine solution, 5C4466P, Baxter Healthcare Corporation. For dialysis. Intended to isolate the Easy-Lock connector of the solution transfer set.
Reason
leaking pouches
Identifiers
| code_info | Lot Number GD893891 |
|---|
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-1565-2013%22
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