Device recall event
Recall event 89376: GE Healthcare, LLC
FDA device recall · Class II · Open, Classified
Key facts
| Recall event number | 89376 |
|---|---|
| Recalling firm | GE Healthcare, LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K001773, K012200, K012875, K013636, K022397, K030874, K032795, K040444, K041476, K052293, K052978, K103238 and 32 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