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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
PMA Number: P050023/S087
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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 Iperia 7, DR-T, DF-1, ProMRI REF 392409, UDI: 04035479128777 - Product Usage: intended to ... 2 04/21/2021 BIOTRONIK Inc
BIOTRONIK IPERIA 7,VR-T, DX, DF-1, ProMRI, REF 393032, UDI: 04035479129477 - Product Usage: intended... 2 04/21/2021 BIOTRONIK Inc
BIOTRONIK INVENTRA 7, VR-T DX DF-1 ProMRI, REF 399436, UDI: 04035479136314 - Product Usage: intende... 2 04/21/2021 BIOTRONIK Inc
BIOTRONIK ILIVIA 7, VR-T DF4 ProMRI, REF 404626, UDI: 04035479142131 - Product Usage: intended to p... 2 04/21/2021 BIOTRONIK Inc
BIOTRONIK IPERIA 7, DR-T DF4 ProMRI, REF 392423, UDI: 04035479128913 - Product Usage: intended to pr... 2 04/21/2021 BIOTRONIK Inc
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