Device recall event
Recall event 71721: Customed, Inc
FDA device recall · Class II · Terminated
Key facts
| Recall event number | 71721 |
|---|---|
| Recalling firm | Customed, Inc |
| Recall class | Class II |
| Status | Terminated |
| 510(k) numbers | K902029, K902030, K902031, K902032, K902191, K902271, K902274, K902886, K904693, K904694, K924809, K925015 and 5 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