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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K123392
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Product Description
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Recall
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FDA Recall
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Avenir Muller Stem; Item Number: 01.06010.003, Lot Number: 2904368, UDI: (01) 00889024479494 (17) 22... 2 04/26/2018 FEI # 3005233524
Zimmer GmbH
Avenir Muller Stem; Item Number: 01.06010.104, Lot Number: 2905496, UDI: (01)00889024479500 (17)2204... 2 04/26/2018 FEI # 3005233524
Zimmer GmbH
Avenir M®ller Stem 4 Standard Avenir M®ller Stem 6 Lateral Hip joint metal/ceramic/polymer semi-... 2 07/26/2016 FEI # 3005233524
Zimmer Gmbh
Avenir® Muller Stem Standard, uncemented HA, 1, Taper 12/14 Item Number: 01.06010.001 - Product Usag... 2 12/20/2018 FEI # 3005233524
Zimmer GmbH
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