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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/S058
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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BIOTRONIK Ilestro 7 DR-T, DF-1, REF383562, UDI: 04035479125189 - Product Usage: intended to provide ... 2 04/21/2021 BIOTRONIK Inc
BIOTRONIK Ilestro 7 VR-T, DF-1, REF 383578, UDI: 04035479125349 - Product Usage: intended to provide... 2 04/21/2021 BIOTRONIK Inc
BIOTRONIK Iforia 7,DR-T, DF-1,REF 390064, UDI: 04035479126926 - Product Usage: intended to provide v... 2 04/21/2021 BIOTRONIK Inc
BIOTRONIK Iforia 7, vr-T, DX, DF-1,REF 390090, UDI: 04035479127176 - Product Usage: intended to prov... 2 04/21/2021 BIOTRONIK Inc
BIOTRONIK Ilestro 7 VR-T DX, DF-1, REF 383594, UDI: 04035479125509 - Product Usage: intended to prov... 2 04/21/2021 BIOTRONIK Inc
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