Covidien recalls Puritan Bennett 980 Series ventilators with specific serial numbers due to a capacitor assembly error that may cause the device to become inoperable during use. Affected units include 14 specific serial numbers.
Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
Covidien is recalling Puritan Bennett 980 Series ventilators with certain serial numbers because a manufacturing error in the capacitor could cause the device to stop working during use. This is serious for medical equipment that requires reliable operation.
A manufacturing assembly error caused a capacitor in the ventilator to be installed incorrectly. This error may lead to the device becoming inoperable during use, which could disrupt critical medical treatment for patients.
Healthcare providers using the Puritan Bennett 980 Series ventilators with the listed serial numbers are most at risk. Patients relying on these ventilators could face interruptions in care if the device becomes inoperable.
Check if your ventilator has the serial numbers listed: 35B1700409, 35B1700443, 35B1700457, 35B1700462, 35B1700473, 35B1700476, 35B1700483, 35B1700487, 35B1700490, 35B1700511, 35B1700552, 35B1700567, 35B1700569, 35B1700570.
Verify your ventilator's serial number against the list of affected units provided in the recall notice.
A manufacturing assembly error caused a capacitor to be installed incorrectly, which may cause the device to become inoperable during use.
Check your serial number against the list of affected units. If it matches, contact Covidien for further instructions.
The recall record does not specify a remedy, so no immediate fix is provided. Affected units should be checked and contacted for guidance.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-0340-2022 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-0340-2022 from Covidien. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
