Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K200795 |
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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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ICM LNQ22 LINQ II, Model LNQ22; Insertable Cardiac Monitor | 2 | 12/01/2023 | Medtronic Inc. |
LINQ II Insertable Cardiac Monitor | 2 | 03/11/2022 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Medtronic LINQ II Model Number # LNQ22 Insertable Cardiac Monitor Sterile EO Rx Only | 2 | 07/14/2021 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
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