Medline Kits: 1) VALVE PACK-LF — Class I medical device recall Z-2670-2025
Ongoing recall by Medline Industries, LP, reported 2025-10-08, distributed nationwide. The kits contain certain lots of cannula products where the catheter may not retain its shape.
| Recall number | Z-2670-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries, LP, Northfield, IL, United States |
| Recall initiated | 2025-08-21 |
| Classified | 2025-10-01 |
| Reported by FDA | 2025-10-08 |
| Distributed | Nationwide (US) |
| Quantity | 828 units |
| UPC / GTIN / UDI-DI | 10195327177966, 10195327678227, 40195327177967, 40195327678228 |
| Lot numbers | 24DMC189, 24DMG366, 24EMC463, 24GMJ353, 24IMB824, 24KME116, 25AMB610, 25BMJ241, 25CMI425, 25EMD672, 25GMD016 |
| Model numbers | DYNJ0415366P, DYNJ0415366Q |
Product
Medline Kits: 1) VALVE PACK-LF, Model Number: DYNJ0415366P; 2) VALVE PACK-LF, Model Number: DYNJ0415366Q
Reason for recall
The kits contain certain lots of cannula products where the catheter may not retain its shape.
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-2670-2025. 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.