Medline Convenience Kits: 1) NAIL KIT — Class II medical device recall Z-1432-2026
Ongoing recall by Medline Industries, LP, reported 2026-03-04, distributed nationwide. Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured produc
| Recall number | Z-1432-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries, LP, Northfield, IL, United States |
| Recall initiated | 2026-01-05 |
| Classified | 2026-02-20 |
| Reported by FDA | 2026-03-04 |
| Distributed | Nationwide (US) |
| Countries outside the US | BM, BS, KY |
| Quantity | 1,640 units |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 10889942819362, 40889942819363 |
| Lot numbers | 23IBF119, 23IBU998, 23JBV524, 24DBB718, 24DBJ364, 25ABU209, 25CBJ329, 25CBS147 |
| Model numbers | POD14214 |
Product
Medline Convenience Kits: 1) NAIL KIT, Model Number: POD14214
Reason for recall
Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1432-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.