Device recall event
Recall event 37887: Abbott Laboratories
FDA device recall · Class II · Terminated
Key facts
| Recall event number | 37887 |
|---|---|
| Recalling firm | Abbott Laboratories |
| Recall class | Class II |
| Status | Terminated |
| 510(k) numbers | K041811, K953943, K954045, K954318, K954575, K954576, K963926, K964020, K972232, K983848 |
| PMA numbers | P050049, P060003, P060009, P060012, P780012, P790019, P970027 |
At a glance
- 10–99 Recalled products (Z-numbers)
- 10–99 Linked 510(k)s
- 10–99 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