Reported May 4, 2022 · Ongoing

Puritan Bennett 980 Series Ventilator

Medtronic formerly Covidien

High riskUsing this product could cause serious injury, illness or death — stop using it now.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Medtronic formerly Covidien · Michael Collins Road, Mervue Ind. Park · Galway · N/A

Is this the product you have?

  • Puritan Bennett 980 Series Ventilator
Lot codes and dates
  • Lot/Serial Number | Product GTIN/MATNR

    2,505 of 2,505 codes

    • 35B2014306
    • 10884521171633
    • 35B2014309
    • 10884521171633
    • 35B2014312
    • 10884521171633
    • 35B2014314
    • 10884521171633
    • 35B1500319
    • 10884521201408
    • 35B1500321
    • 10884521201521
    • 35B1500322
    • 10884521201408
    • 35B1500323
    • 10884521201408
    • 35B1500324
    • 10884521201408
    • 35B1500718
    • 10884521201408
    • 35B1500744
    • 10884521201408
    • 35B1500758
    • 10884521201408
    • 35B1500773
    • 10884521201408
    • 35B1502000
    • 10884521212251
    • 35B1502094
    • 10884521201354
    • 35B1502099
    • 10884521201354
    • 35B1502104
    • 10884521201354
    • 35B1502172
    • 10884521201224
    • 35B1600140
    • 10884521201224
    • 35B1600170
    • 10884521201224
    • 35B1600182
    • 10884521201224
    • 35B1600188
    • 10884521201224
    • 35B1600198
    • 10884521201224
    • 35B1600202
    • 10884521201224
    • 35B1600203
    • 10884521201224
    • 35B1600204
    • 10884521201224
    • 35B1600209
    • 10884521201224
    • 35B1600211
    • 10884521201224
    • 35B1600213
    • 10884521212251
    • 35B1600216
    • 10884521201224
Amount recalled
18,508 OUS; 18,412 US

Where it was sold

  • Nationwide

Why it was recalled

Stop using this product now

The audible alarm may not sound and/or the omni-directional LED visual alarm may not display during alarm states. Delayed awareness of alarm states may lead to delayed response or a delay of treatment, potentially resulting in hypoxia, dyspnea, cardiac arrest, or death.

Using this product could cause serious injury, illness or death — stop using it now.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:40 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.