Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K954465 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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FMS 3.5mm Ultra-Aggressive Cutter Shaver Blades; Product Code: 287325 Intended to provide control... | 2 | 01/15/2016 | DePuy Mitek, Inc., a Johnson & Johnson Co. |
DePuy Mitek FMS Outflow Tubing with One-Way valve Product Code:284649 Product Usage: The Inter... | 2 | 11/08/2013 | DePuy Mitek, Inc., a Johnson & Johnson Co. |
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