Device recall event
Recall event 25088: Baxter Healthcare Corp.
FDA device recall · Class I · Terminated
Key facts
| Recall event number | 25088 |
|---|---|
| Recalling firm | Baxter Healthcare Corp. |
| Recall class | Class I |
| Status | Terminated |
| 510(k) numbers | K791496, K811078, K860746, K915390, K921899, K924721, K925126, K984381 |
At a glance
- 10–99 Recalled products (Z-numbers)
- 1–9 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