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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/S079
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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BIOTRONIK INVENTRA 7, VR-T DX DF-1, REF 399437, UDI: 04035479136321 - Product Usage: intended to pr... 2 04/21/2021 BIOTRONIK Inc
BIOTRONIK ITREVIA 7, DR-T QP DF-1, REF 392412, UDI: 04035479128807 - Product Usage: intended to pro... 2 04/21/2021 BIOTRONIK Inc
BIOTRONIK ITREVIA 7, VR-T DF-1, REF 393040, UDI: 04035479129552 - Product Usage: intended to provide... 2 04/21/2021 BIOTRONIK Inc
BIOTRONIK ITREVIA 7, VR-T DF-4, REF 393041, UDI: 04035479129569 - Product Usage: intended to provide... 2 04/21/2021 BIOTRONIK Inc
BIOTRONIK ITREVIA 7, VR-T DX DF-1, REF 393037, UDI: 04035479129521 - Product Usage: intended to prov... 2 04/21/2021 BIOTRONIK Inc
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