Device recall event
Recall event 97816: B Braun Medical Inc
FDA device recall · Class II · Open, Classified
Key facts
| Recall event number | 97816 |
|---|---|
| Recalling firm | B Braun Medical Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K022895, K032393, K060231, K083723, K111016, K140311, K142036, K153293, K170595, K191658, K202618, K760383 and 10 more |
At a glance
- 100–999 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