---
title: "Puritan Bennett 980 Series Ventilator, 980X2ESDIEC — FDA record Z-0351-2022 | Is It on Recall"
description: "Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use."
url: https://isitonrecall.com/recall/fda-device-z-0351-2022-puritan-bennett-980-series-ventilator-980x2esdiec/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# 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](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## 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](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0351-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | GTIN/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.

- [Alaska](https://isitonrecall.com/state/alaska/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## 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.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0351-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Covidien Llc records](https://isitonrecall.com/brand/covidien-llc/)
