Device recall event
Recall event 83783: Zimmer Biomet, Inc.
FDA device recall · Class II · Terminated
Key facts
| Recall event number | 83783 |
|---|---|
| Recalling firm | Zimmer Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| 510(k) numbers | K003397, K010635, K010827, K013503, K023409, K030055, K043100, K051843, K062998, K081244, K112905, K172502 and 1 more |
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