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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
Recall Number: Z-1048-2018
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CR-FLEX POR FEM F-L CR-FLEX POR FEM F-R MINUS CR-FLEX POR FEM G-L This device is indicated for ... 2 03/14/2018 FEI # 1000220733
Zimmer Biomet, Inc.
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