Device recall
Z-3267-2011: ANGIODYNAMICS UNI*FUSE INFUSION SYSTEM WITH COOPER WIRE, Catalog No./REF…
FDA device recall · Class II · Angiodynamics Worldwide Headquarters
Key facts
| Recall number (Z-number) | Z-3267-2011 |
|---|---|
| Recall event | 59820 |
| Product | ANGIODYNAMICS UNI*FUSE INFUSION SYSTEM WITH COOPER WIRE, Catalog No./REF 12401819, CATHETER SIZE 4F, CATHETER LENGTH 90 cm, INFUSION LENGTH 20 cm, OCCLUSION WIRE SIZE .035 in., STERILE, AngioDynamics Inc., 603 Queensbury Avenue, Queensbury, NY 12804 |
| Product code | KRA |
| Recalling firm | Angiodynamics Worldwide Headquarters |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 18, 2012 |
| 510(k) numbers | K951509 |
| FEI number | 3008319439 |
At a glance
- 1–9 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