Medical Device Recalls
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11 to 11 of 11 Results
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-1621-2018 - Capio RP; Model #M0068321010. Intended for use in general suturing applications during open surgery to assist in the placement of suture material in tissues at the operative site. | 2 | 05/04/2018 |
FEI # 3005099803 Boston Scientific Corporation |
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