Medical Device Recalls
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1 to 4 of 4 Results
PMA Number: P900056 |
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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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ROTAWIRE Drive and wireClip Torquer, ROTAWIRE Drive Floppy | 2 | 04/12/2022 | Boston Scientific Corporation |
ROTAWIRE Drive and wireClip Torquer, ROTAWIRE Drive Extra Support | 2 | 04/12/2022 | Boston Scientific Corporation |
RotaWire Elite and wireClip Torquer, Guidewire and Guidewire Manipulation Device, Floppy. REF H8022... | 1 | 11/13/2015 | Boston Scientific Corporation |
RotaWire Elite and wireClip Torquer, Guidewire and Guidewire Manipulation Device, Extra Support. RE... | 1 | 11/13/2015 | Boston Scientific Corporation |
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