Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Z-0282-2022 - Medtronic CareLink SmartSync Device Manager application software (D00U005) used by the following Medtronic Cobalt and Crome implantable cardioverter defibrillators (ICDs) and cardiac resynchronization... | 2 | 11/24/2021 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
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