Device recall event
Recall event 93711: St. Jude Medical, Atrial Fibrillation Division, Inc.
FDA device recall · Class II · Open, Classified
Key facts
| Recall event number | 93711 |
|---|---|
| Recalling firm | St. Jude Medical, Atrial Fibrillation Division, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| PMA numbers | P130026 |
At a glance
- 1–9 Recalled products (Z-numbers)
- None Linked 510(k)s
- 1–9 Recall events for this firm
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recall events
A recall event groups every recalled product (Z-number) from one recall action by a firm. Class I recalls involve a reasonable probability of serious harm; Class III recalls are unlikely to cause harm.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database