RecallRadar

FDA Device recall Z-0342-2022

Puritan Bennett 980 Series Ventilator, 980U1ENASAA

On 2021-12-15 the FDA classified a Class I recall of Puritan Bennett 980 Series Ventilator, 980U1ENASAA 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

AgencyFDA Device
Recall numberZ-0342-2022
ClassificationClass I
Statusterminated
Initiated2021-11-04
Published2021-12-15
Last updated2026-09-13 11:56 UTC
CompanyCovidien
DistributionUS

Product

Puritan Bennett 980 Series Ventilator, 980U1ENASAA

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 - 10884521201385 Serial Numbers: 35B1700252 35B1700365 35B1700399 35B1700407 35B1700489 35B1700505 35B1700513…GTIN/UDI - 10884521201385 Serial Numbers: 35B1700252 35B1700365 35B1700399 35B1700407 35B1700489 35B1700505 35B1700513 35B1700555 35B1700557 35B1700562 35B1700563 35B1700565 35B1700566 35B1700605 35B1700612 35B1700634 35B1700651 35B1700662 35B1700663

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-0342-2022%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.