Device recall
Z-0599-03: Bard Stinger M Ablation Catheters: Item Numbers 210001M 218501M 210002M 218502M…
FDA device recall · Class II · C. R.Bard, Inc./Electrophysiology Division
Key facts
| Recall number (Z-number) | Z-0599-03 |
|---|---|
| Recall event | 25401 |
| Product | Bard Stinger M Ablation Catheters: Item Numbers 210001M 218501M 210002M 218502M 210003M 218503M 210004M 218504M 210005M 218505M 210006M 218506M 210007M 218507M 210015M 218516M 210016M 218518M 210017M 218519M 210018M 218520M 210019M 218521M 210020M 218523M 210023M 218524M 210024M 218525M 210025M… |
| 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