Device recall event
Recall event 30104: Becton Dickinson & Company
FDA device recall · Class II · Terminated
Key facts
| Recall event number | 30104 |
|---|---|
| Recalling firm | Becton Dickinson & Company |
| Recall class | Class II |
| Status | Terminated |
| 510(k) numbers | BK040030, K002456, K023075, K040030, K771370, K901449, K921806, K931368, K940905, K960250, K991702 |
At a glance
- 1–9 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