Puritan Bennett 980 Series Ventilator, 980X2ESDIEC — FDA record Z-0351-2022

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Nov 4, 2021. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
Puritan Bennett 980 Series Ventilator, 980X2ESDIEC
Reason
Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
Classification
Class I
Recalling firm
Covidien Llc
Quantity
278 total
Agency-reported status
Terminated
Source record identifier
Z-0351-2022

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityGTIN/UDI - 10884521174177 Serial Numbers: 35B1700627 35B1700628 35B1700629 35B1700630 35B1700631 35B1700632

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

Worldwide distribution - US Nationwide.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Dec 15, 2021
Recall initiation date
Nov 4, 2021
Center classification date
Dec 9, 2021
Termination date
Jul 9, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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