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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-0237-2022
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OMNI K2 Hip Stem, Manufacturer's Product Code 130006 The OMNI K2 Hip Stem is intended for use as th... 2 11/16/2021 FEI # 3008342029
OmniLife Science
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