FDA Device recall Z-1269-2015
MiniCap with Povidone-Iodine Solution, item number 5C4466P, for hemodialysis
- FDA Device
- Class II
- completed
- Published 2015-03-25
On 2015-03-25 the FDA classified a Class II recall of MiniCap with Povidone-Iodine Solution, item number 5C4466P, for hemodialysis by Baxter Healthcare, citing product may have separating or protruding sponges.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1269-2015 |
| Classification | Class II |
| Status | completed |
| Initiated | 2015-01-22 |
| Published | 2015-03-25 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
Product
MiniCap with Povidone-Iodine Solution, item number 5C4466P, for hemodialysis.
Reason
Product may have separating or protruding sponges
Identifiers
| code_info | Lot Numbers: GD896845, Exp. 10/2015; GD897371, Exp. 01/2016; GD896936, Exp. 10/2015; GD897124, Exp. 11/2015; GD897165,…Lot Numbers: GD896845, Exp. 10/2015; GD897371, Exp. 01/2016; GD896936, Exp. 10/2015; GD897124, Exp. 11/2015; GD897165, Exp. 12/2015; GD897157, Exp. 12/2015; GD896944, Exp. 11/2015; GD896837, Exp. 10/2015 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1269-2015%22
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