Device recall
Z-0600-03: Bard Stinger S Ablation Catheter: Item Numbers 210001S 218501S 6210015S 210002S…
FDA device recall · Class II · C. R.Bard, Inc./Electrophysiology Division
Key facts
| Recall number (Z-number) | Z-0600-03 |
|---|---|
| Recall event | 25401 |
| Product | Bard Stinger S Ablation Catheter: Item Numbers 210001S 218501S 6210015S 210002S 218502S 6210016S 210003S 218503S 6210017S 210004S 218504S 6210018S 210005S 218505S 6210019S 210006S 218506S 6210020S 210007S 218507S 210015S 218516S 210016S 218518S 210017S 218519S 210018S 218520S 210019S 218521S 210020S… |
| Recalling firm | C. R.Bard, Inc./Electrophysiology Division |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 3, 2012 |
| FEI number | 1000120754 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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