Device recall event
Recall event 87329: Cordis Corporation
FDA device recall · Class I · Completed
Key facts
| Recall event number | 87329 |
|---|---|
| Recalling firm | Cordis Corporation |
| Recall class | Class I |
| Status | Completed |
| PMA numbers | P030047 |
At a glance
- 1–9 Recalled products (Z-numbers)
- None 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