Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K110555 |
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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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Active Articulation ArComXL Polyethylene Bearings Active Articulation ArComXL Bearings item XL-2001... | 2 | 01/13/2017 | Zimmer Biomet, Inc. |
RingLoc ArComXL Highly Crosslinked Polyethylene Liners ArComXL High Wall +3mm Liners Size 23 item X... | 2 | 01/13/2017 | Zimmer Biomet, Inc. |
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