Device recall event
Recall event 52076: Medtronic Inc. Cardiac Rhythm Disease Managment
FDA device recall · Class I · Terminated
Key facts
| Recall event number | 52076 |
|---|---|
| Recalling firm | Medtronic Inc. Cardiac Rhythm Disease Managment |
| Recall class | Class I |
| Status | Terminated |
| PMA numbers | P890003, P890003S065, P970012, P980035, P980035S002, P980035S014, P980035S029, P980035S031, P980035/S4, P980035/S9 |
At a glance
- 10–99 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