Device recall event
Recall event 87074: Aomori Olympus Co., Ltd.
FDA device recall · Class II · Terminated
Key facts
| Recall event number | 87074 |
|---|---|
| Recalling firm | Aomori Olympus Co., Ltd. |
| Recall class | Class II |
| Status | Terminated |
| 510(k) numbers | K023272, K050503, K060243, K091495, K092309, K153625, K171158, K172734, K902735, K933200, K950729, K955650 and 1 more |
At a glance
- 100–999 Recalled products (Z-numbers)
- 10–99 Linked 510(k)s
- 1–9 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