Medical Device Recalls
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1 result found
PMA Number: P970004/S268 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| InterStim(TM) System, Model Numbers: a) TH90G01 b) TH90GFA c) TH90G02 d) TH90G03 Product Usag... | 2 | 06/07/2019 |
FEI # 2182207 Medtronic Neuromodulation |
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