FDA Device recall Z-2074-2014
Baxter MiniCap with Povidone-Iodine Solution, 5C4466P, Baxter Healthcare Corporation
- FDA Device
- Class II
- terminated
- Published 2014-07-23
On 2014-07-23 the FDA classified a Class II recall of Baxter MiniCap with Povidone-Iodine Solution, 5C4466P, Baxter Healthcare Corporation by Baxter Healthcare, citing inadequate iodine and packaging related defects.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2074-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-06-17 |
| Published | 2014-07-23 |
| 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.
Reason
Inadequate iodine and packaging related defects.
Identifiers
| code_info | GD895771 |
|---|
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-2074-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.