Device recall event
Recall event 49510: Sterilmed Inc
FDA device recall · Class II · Terminated
Key facts
| Recall event number | 49510 |
|---|---|
| Recalling firm | Sterilmed Inc |
| Recall class | Class II |
| Status | Terminated |
| 510(k) numbers | K003857, K012523, K012556, K012571, K012574, K012579, K012581, K012598, K012678, K012679, K012682, K012684 and 10 more |
At a glance
- 10–99 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