Medical Device Recalls
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11 to 17 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, 980X1JADIJJ | 1 | 12/09/2021 | Covidien, LP |
| Puritan Bennett 980 Series Ventilator, 980X1PLDIPC | 1 | 12/09/2021 | Covidien, LP |
| Puritan Bennett 980 Series Ventilator, 980X2ESDIEC | 1 | 12/09/2021 | Covidien, LP |
| Puritan Bennett 980 Series Ventilator, 980X3ENDIUU | 1 | 12/09/2021 | Covidien, LP |
| Puritan Bennett 980 Series Ventilator, 980X3JADIJJ | 1 | 12/09/2021 | Covidien, LP |
| Puritan Bennett 980 Series Ventilator, 980A1ENNISB | 1 | 12/09/2021 | Covidien, LP |
| Puritan Bennett 980 Series Ventilator, 980A3ENNISB | 1 | 12/09/2021 | Covidien, LP |
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