Medical Device Recalls
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Related Medical Device Recalls |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-0211-2016 - RotaWire Elite and wireClip Torquer, Guidewire and Guidewire Manipulation Device, Floppy. REF H802223301 (5-pack outer package), REF H802223300 (single unit). The Rotablator rotational atherec... | 1 | 11/13/2015 |
FEI # 3002095335 Boston Scientific Corporation |
| Z-0212-2016 - RotaWire Elite and wireClip Torquer, Guidewire and Guidewire Manipulation Device, Extra Support. REF H802233301 (5-pack outer package), REF H802233300 (single unit). The Rotablator rotational ... | 1 | 11/13/2015 |
FEI # 3002095335 Boston Scientific Corporation |
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