Halyard convenience kits containing recalled Medline Namic… — Class I medical device recall Z-2796-2026
Ongoing recall by AVID Medical, Inc., reported 2026-08-12, distributed nationwide. Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufac
| Recall number | Z-2796-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | AVID Medical, Inc., Toano, VA, United States |
| Recall initiated | 2026-04-30 |
| Classified | 2026-07-31 |
| Reported by FDA | 2026-08-12 |
| Distributed | Nationwide (US) |
| Quantity | 5,168 kits |
| Reason classes | specification failure |
| UPC / GTIN / UDI-DI | 10809160377314 |
| Lot numbers | 1573593, 1583827, 1609541, 1612134, 1612516, 1619132, 1623384, 1627013, 1635459, 1672306, 1675159 |
Product
Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. CARDIAC CATH PACK EAMC1000-05
Reason for recall
Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within fluid path of the Manifolds. Particulate within the fluid path has the potential to be introduced into blood circulation and become lodged within blood vessels.
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-2796-2026. 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.