FDA Device recall Z-1932-2026
LSL Healthcare, IV Start Kit, Model/Catalog Number: 3131
- FDA Device
- Class II
- ongoing
- Published 2026-04-29
On 2026-04-29 the FDA classified a Class II recall of LSL Healthcare, IV Start Kit, Model/Catalog Number: 3131 by Lsl Healthcare, citing medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1932-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-03-09 |
| Published | 2026-04-29 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Lsl Healthcare |
| Distribution | US |
Product
LSL Healthcare, IV Start Kit, Model/Catalog Number: 3131
Reason
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
Identifiers
| code_info | Lot Code: Model No. 3131; UDI-DI 00661392054271; Lot#6A3139, Expiration Date 01/21/2028 GTIN: (01)00661392054271(10)6A3139(17)280121 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1932-2026%22
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