Device recall
Z-1344-2016: NAMIC CONVENIENCE KIT RENOWN REGIONAL MEDICAL CENTER, REF Catalog No. 65230029…
FDA device recall · Class II · AngioDynamics Inc.
Key facts
| Recall number (Z-number) | Z-1344-2016 |
|---|---|
| Recall event | 72957 |
| Product | NAMIC CONVENIENCE KIT RENOWN REGIONAL MEDICAL CENTER, REF Catalog No. 65230029, UPN Product No. H965652300290, Product is packed as a box of 30 pieces, box label contains UPN Product No. H965652300291 Product Usage - This needle is intended to be placed over the guidewire to enlarge the opening in… |
| Product code | OEZ |
| Recalling firm | AngioDynamics Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 16, 2017 |
| FEI number | 3017892510 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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