Medical Device Recalls
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1 to 2 of 2 Results
Related Medical Device Recalls |
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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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Z-0391-2022 - Medical Device Identification Cards associated with Astra XT DR Implantable pulse generator | 2 | 12/16/2021 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Z-0390-2022 - Medical Device Identification Cards associated with Sprint Quattro Lead, Product/CFN 6935M72 | 2 | 12/16/2021 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
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