Device recall
Z-1345-2016: NAMIC CONVENIENCE KIT HOLYOKE HOSPITAL SPECIAL PROCEDURE KIT, REF Catalog No…
FDA device recall · Class II · AngioDynamics Inc.
Key facts
| Recall number (Z-number) | Z-1345-2016 |
|---|---|
| Recall event | 72957 |
| Product | NAMIC CONVENIENCE KIT HOLYOKE HOSPITAL SPECIAL PROCEDURE KIT, REF Catalog No. 60080094, UPN Product No. H749600800941 Product Usage - This needle is intended to be placed over the guidewire to enlarge the opening in the vessel, and is then removed before sliding the catheter over the guidewire |
| 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