Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K210392 |
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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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v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate Claris System, Model H700123. The WorkMate... | 2 | 06/14/2021 | Abbott Laboratories Inc. (St Jude Medical) |
WorkMate Claris v.1.2 Upgrade Kits, Model Numbers H800007 and H800012 | 2 | 06/14/2021 | Abbott Laboratories Inc. (St Jude Medical) |
v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate Claris" System Display, Model H700124, T... | 2 | 06/14/2021 | Abbott Laboratories Inc. (St Jude Medical) |
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