Medical Device Recalls
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1 to 3 of 3 Results
PMA Number: P930038 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Angio-Seal Evolution Vascular Closure Device, Cat. No. C610135 | 2 | 06/29/2018 | Terumo Medical Corp |
The affected device is labeled Angio-Seal Vascular Closure Device 6F VIP Platform, model 610130. Th... | 3 | 11/07/2006 | St. Jude Medical / Daig Division |
Angio-Seal Vascular Closure Device. Ref 610109. 6F STS Platform. Sterilized by gamma radiation. ... | 2 | 03/25/2006 | St. Jude Medical / Daig Division |
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