Device recall
Z-0966-2022: Puritan Bennett 980 Series Ventilator
FDA device recall · Class I · Medtronic formerly Covidien
Key facts
| Recall number (Z-number) | Z-0966-2022 |
|---|---|
| Recall event | 89820 |
| Product | Puritan Bennett 980 Series Ventilator |
| Product code | CBK |
| Recalling firm | Medtronic formerly Covidien |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K193056 |
| FEI number | 3002807850 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database