Device recall event
Recall event 36522: Arrow International Inc
FDA device recall · Class II · Terminated
Key facts
| Recall event number | 36522 |
|---|---|
| Recalling firm | Arrow International Inc |
| Recall class | Class II |
| Status | Terminated |
| 510(k) numbers | K790882, K875214, K882230, K903691, K911055, K921379, K921475, K922434, K925373, K926011, K932447, K933316 and 7 more |
At a glance
- 10–99 Recalled products (Z-numbers)
- 10–99 Linked 510(k)s
- 100–999 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