FDA DevicesClass I
Custom Convenience Kit containing recalled Medline Namic Angiographic Control Sy...
Published: May 20, 2026Recall ID: Z-2066-2026Category: devicesCountry: US
Reason for Recall / Hazard
Affected kits contain Medline Namic RA Syringes, which are recalled by their manufacturer due to risk of syringe rotating adapter unwinding during use, which may result in a loose connection or full disconnection between syringe and manifold. If unwinding occurs, there is a potential for biohazard exposure, blood loss, infection. or air embolism.
Product Description & Identification
Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes with Rotating Adapter (Namic RA Syringes) Angio Pack Part numbers AMS6908E, AMS6908F
Affected Products
Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes with Rotating Adapter (Namic RA Syringes) Angio Pack Part numbers AMS6908E, AMS6908F
Additional Source Details
| Field | Value |
|---|---|
| City | Billings |
| State | MT |
| Event id | 98741 |
| Address 1 | 1602 4th Ave N |
| Code info | Pack AMS6908E UDI-DI B098AMS6908E0 Lot 214875 Pack AMS6908F UDI-DI B098AMS6908F0 Lots 215436, 225001, 226706, 234088 |
| Postal code | 59101-1521 |
| Report date | 20260520 |
| Product type | Devices |
| Product quantity | 150 kits (US only) |
| Reason for recall | Affected kits contain Medline Namic RA Syringes, which are recalled by their manufacturer due to risk of syringe rotating adapter unwinding during use, which may result in a loose connection or full disconnection between syringe and manifold. If unwinding occurs, there is a potential for biohazard exposure, blood loss, infection. or air embolism. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260402 |
| Initial firm notification | |
| Center classification date | 20260508 |
Overview
- Recalling FirmWindstone Medical Packaging, Inc.
- StatusOngoing
- Risk LevelClass I
- DistributionUS Nationwide distribution in the state of Arizona.