Device recall event
Recall event 66500: Zimmer, Inc.
FDA device recall · Class II · Terminated
Key facts
| Recall event number | 66500 |
|---|---|
| Recalling firm | Zimmer, Inc. |
| Recall class | Class II |
| Status | Terminated |
| 510(k) numbers | K030265, K032367, K043101, K060710, K063303, K082527, K083654, K112885, K792022, K830121, K830196, K830196¿VERS and 26 more |
| PMA numbers | P040048 |
At a glance
- 10–99 Recalled products (Z-numbers)
- 10–99 Linked 510(k)s
- 100–999 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