Device recall
Z-2066-2026: Custom Convenience Kit containing recalled Medline Namic Angiographic Control…
FDA device recall · Class I · Windstone Medical Packaging, Inc.
Key facts
| Recall number (Z-number) | Z-2066-2026 |
|---|---|
| Recall event | 98741 |
| Product | Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes with Rotating Adapter (Namic RA Syringes) Angio Pack Part numbers AMS6908E, AMS6908F |
| Product code | LRO |
| Recalling firm | Windstone Medical Packaging, Inc. |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 1000125955 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database