Device recall event
Recall event 93687: Howmedica Osteonics Corp.
FDA device recall · Class II · Open, Classified
Key facts
| Recall event number | 93687 |
|---|---|
| Recalling firm | Howmedica Osteonics Corp. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K011643, K012172, K030978, K032163, K032418, K041591, K051948, K052917, K863668, K884398, K894403, K914565 and 7 more |
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