[Recalled] Covidien Puritan Bennett 980 Ventilator, Rx ONLY, Made in Ireland., Covidien LLC, USA. REF 980X1ENDIUU. — Covidien is recalling certain Puritan Bennett 980 Ventilator Systems due to a b… | FDA 2014-10-01
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | Covidien Puritan Bennett 980 Ventilator, Rx ONLY, Made in Ireland., Covidien LLC, USA. REF 980X1ENDIUU. |
|---|---|
| Brand / manufacturer | Nellcor Puritan Bennett Inc. (dba Covidien LP) |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0180-2015 |
| Country of notice | United States |
| Risk level | Class I |
| Hazard type | recall |
| Notice date | 01 October 2014 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Covidien is recalling certain Puritan Bennett 980 Ventilator Systems due to a blacklight inverter PCBA where a capacitor component can fail, causing a dim but functional screen and thermal odor.
This Class I recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Stop using the product immediately and follow the authority's remedy (return, repair, or disposal).
Read the full official notice →
Related recalls from Nellcor Puritan Bennett Inc. (dba Covidien LP)
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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