Device recall event
Recall event 78706: Zimmer Biomet, Inc.
FDA device recall · Class II · Terminated
Key facts
| Recall event number | 78706 |
|---|---|
| Recalling firm | Zimmer Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| 510(k) numbers | K023211, K030079, K031061, K033034, K033363, K041100, K060370, K070214, K070695, K071107, K072619, K833991 and 9 more |
| PMA numbers | P060037 |
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