Device recall event
Recall event 85297: WELCH ALLYN, INC/MORTARA
FDA device recall · Class II · Terminated
Key facts
| Recall event number | 85297 |
|---|---|
| Recalling firm | WELCH ALLYN, INC/MORTARA |
| Recall class | Class II |
| Status | Terminated |
| 510(k) numbers | K041607, K050896, K081800, K092663, K093339, K100127, K101115, K101403, K102206, K152944, K160685, K173765 and 1 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