Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K180149 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Covidien Sonicision Battery Charger-intended to charge the Sonicision Reusable Battery Pack and to p... | 2 | 12/03/2021 | Covidien Llc |
Covidien Sonicision Reusable Generator-converts electrical power from the battery pack to ultrasonic... | 2 | 08/10/2021 | Covidien Llc |
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