FDA Device recall Z-2796-2026
Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds
- FDA Device
- Class I
- ongoing
- Published 2026-08-12
On 2026-08-12 the FDA classified a Class I recall of Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds by Avid Medical, citing 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 Manifo….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2796-2026 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2026-04-30 |
| Published | 2026-08-12 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Avid Medical |
| Distribution | US |
Product
Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. CARDIAC CATH PACK EAMC1000-05
Reason
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.
Identifiers
| code_info | UDI-DI 10809160377314 Lots 1573593 1583827 1609541 1612134 1612516 1619132 1623384 1627013 1635459 1672306 1675159 |
|---|
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-2796-2026%22
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