Medline medical convenience kits packaged as: 1) POWERGLIDE DRESSING… — Class II medical device recall Z-1331-2026
Ongoing recall by Medline Industries, LP, reported 2026-02-18, distributed nationwide. Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPre
| Recall number | Z-1331-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries, LP, Northfield, IL, United States |
| Recall initiated | 2025-12-24 |
| Classified | 2026-02-09 |
| Reported by FDA | 2026-02-18 |
| Distributed | Nationwide (US) |
| Quantity | 7,380 kits |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 10193489437041, 10889942582013 |
| Lot numbers | 25EBE082, 25EBP737 |
Product
Medline medical convenience kits packaged as: 1) POWERGLIDE DRESSING CHANGE KIT, Kit SKU DYNDH1576; 2) CENTRAL LINE TRAY W/ CHLRP SWB, Kit SKU RWM-DC57KC.
Reason for recall
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
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-1331-2026. 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.