Device recall event
Recall event 99096: Bard Access Systems, Inc.
FDA device recall · Class II · Open, Classified
Key facts
| Recall event number | 99096 |
|---|---|
| Recalling firm | Bard Access Systems, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K001901, K030268, K091324, K102159, K133456, K141531, K153393, K162900, K180548, K201452, K210264, K213203 and 1 more |
At a glance
- 10–99 Recalled products (Z-numbers)
- 10–99 Linked 510(k)s
- 1–9 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