Device recall event
Recall event 98793: ARROW INTERNATIONAL, LLC
FDA device recall · Class I · Open, Classified
Key facts
| Recall event number | 98793 |
|---|---|
| Recalling firm | ARROW INTERNATIONAL, LLC |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K001587, K002507, K003006, K011761, K021120, K042126, K071538, K103658, K112896, K113277, K121403, K122027 and 29 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