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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
PMA Number: P980023/S093
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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BIOTRONIK ILIVIA NEO 7 VR-T DF-1 ProMRI, REF 429531, UDI: 04035479156763 - Product Usage: intended t... 2 04/21/2021 BIOTRONIK Inc
BIOTRONIK INTICA NEO 7 HF-T DF-1 IS-1 ProMRI, REF 429553, UDI: 04035479156831 - Product Usage: inten... 2 04/21/2021 BIOTRONIK Inc
BIOTRONIK ILIVIA NEO 7 DR-T DF-1 ProMRI, REF 429529, UDI: 04035479156749 - Product Usage: intended t... 2 04/21/2021 BIOTRONIK Inc
BIOTRONIK INTICA NEO 7 VR-T DX DF-1 ProMRI, REF 429559, UDI: 04035479156855 - Product Usage: intende... 2 04/21/2021 BIOTRONIK Inc
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