Device recall
Z-0601-03: Bard Stinger SM Ablation Catheter Item Numbers 210001SM 218501SM 210002SM…
FDA device recall · Class II · C. R.Bard, Inc./Electrophysiology Division
Key facts
| Recall number (Z-number) | Z-0601-03 |
|---|---|
| Recall event | 25401 |
| Product | Bard Stinger SM Ablation Catheter Item Numbers 210001SM 218501SM 210002SM 218502SM 210003SM 218503SM 210004SM 218504SM 210005SM 218505SM 210006SM 218506SM 210007SM 218507SM 210015SM 218516SM 210016SM 218518SM 210017SM 218519SM 210018SM 218520SM 210019SM 218521SM 210020SM 218523SM 210023SM 218524SM… |
| 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