Device recall event
Recall event 86777: Boston Scientific Corporation
FDA device recall · Class II · Completed
Key facts
| Recall event number | 86777 |
|---|---|
| Recalling firm | Boston Scientific Corporation |
| Recall class | Class II |
| Status | Completed |
| 510(k) numbers | K003065, K010991, K051052, K060144, K060390, K110946, K111859, K121251, K141485, K152133, K162599, K181741 |
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