Device recall event
Recall event 90731: Mckesson Medical-Surgical Inc. Corporate Office
FDA device recall · Class III · Open, Classified
Key facts
| Recall event number | 90731 |
|---|---|
| Recalling firm | Mckesson Medical-Surgical Inc. Corporate Office |
| Recall class | Class III |
| Status | Open, Classified |
| 510(k) numbers | K014022, K020409, K060804, K070461, K080497, K090453, K101528, K101793, K122446, K132243, K152630, K162508 and 11 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