Device recall event
Recall event 48100: Medtronic Perfusion Systems
FDA device recall · Class II · Terminated
Key facts
| Recall event number | 48100 |
|---|---|
| Recalling firm | Medtronic Perfusion Systems |
| Recall class | Class II |
| Status | Terminated |
| 510(k) numbers | K000430, K031700, K033264, K033416, K071253, K840001, K840002, K842375, K884129, K891687, K924642 |
At a glance
- 10–99 Recalled products (Z-numbers)
- 10–99 Linked 510(k)s
- 10–99 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