Medical Device Recalls
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1 to 10 of 17 Results
510(K) Number: K193056 |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| Puritan Bennett 980 Series Ventilator | 1 | 04/25/2022 | Medtronic formerly Covidien |
| Puritan Bennett 980 Series Ventilator, 980S1ENDICU | 1 | 12/09/2021 | Covidien, LP |
| Puritan Bennett 980 Series Ventilator, 980S3ENDICU | 1 | 12/09/2021 | Covidien, LP |
| Puritan Bennett 980 Series Ventilator, 980U1ENASAA | 1 | 12/09/2021 | Covidien, LP |
| Puritan Bennett 980 Series Ventilator, 980U1ESDIUC | 1 | 12/09/2021 | Covidien, LP |
| Puritan Bennett 980 Series Ventilator, 980U3ESDIUU | 1 | 12/09/2021 | Covidien, LP |
| Puritan Bennett 980 Series Ventilator,980X1ENAIQC | 1 | 12/09/2021 | Covidien, LP |
| Puritan Bennett 980 Series Ventilator, 980X1ENDIPC | 1 | 12/09/2021 | Covidien, LP |
| Puritan Bennett 980 Series Ventilator, 980X1ENDIUU | 1 | 12/09/2021 | Covidien, LP |
| Puritan Bennett 980 Series Ventilator, 980X1ENNISB | 1 | 12/09/2021 | Covidien, LP |
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