FDA Device recall Z-0338-2022
Puritan Bennett 980 Series Ventilator, 980A1ENNISB
- FDA Device
- Class I
- terminated
- Published 2021-12-15
On 2021-12-15 the FDA classified a Class I recall of Puritan Bennett 980 Series Ventilator, 980A1ENNISB by Covidien, citing manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0338-2022 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2021-11-04 |
| Published | 2021-12-15 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Covidien |
| Distribution | US |
Product
Puritan Bennett 980 Series Ventilator, 980A1ENNISB
Reason
Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
Identifiers
| code_info | GTIN/UDI - 10884521201897 Serial Numbers: 35B1700507, 35B1700533, 35B1700539, 35B1700465, 35B1700580, 35B1700530, 35…GTIN/UDI - 10884521201897 Serial Numbers: 35B1700507, 35B1700533, 35B1700539, 35B1700465, 35B1700580, 35B1700530, 35B17005363, 5B1700542, 35B1700509, 35B1701614, 35B1700527, 35B1700537, 35B1700541, 35B1700508 & 35B1701569. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0338-2022%22
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