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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
Recall Date to: 07/25/2014 PMA Number: P030022
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Product Description
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Recall
Class
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FDA Recall
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R3 TM CERAMIC ACETABULAR LINER, BIOLOX® FORTE, 32 MM I.D. 48 MM O.D., REF 71338948, STERILE R, Q... 2 04/22/2011 Smith & Nephew Inc
R3 TM CERAMIC ACETABULAR LINER, BIOLOX® FORTE, 32 MM O.D. 55 MM O.D., REF 71338950, STERILE R, Q... 2 04/22/2011 Smith & Nephew Inc
R3 TM CERAMIC ACETABULAR LINER, BIOLOX® FORTE, 36 MM O.D. 62 MM O.D., REF 71338962, STERILE R, Q... 2 04/22/2011 Smith & Nephew Inc
R3 TM CERAMIC ACETABULAR LINER, BIOLOX® FORTE, 36 MM O.D. 54 MM O.D., REF 71338954, STERILE R, Q... 2 04/22/2011 Smith & Nephew Inc
R3 TM CERAMIC ACETABULAR LINER, BIOLOX® FORTE, 36 MM O.D. 56 MM O.D., REF 71338956, STERILE R, Q... 2 04/22/2011 Smith & Nephew Inc
R3 TM CERAMIC ACETABULAR LINER, BIOLOX® FORTE, 36 MM O.D. 52 MM O.D., REF 71338952, STERILE R, Q... 2 04/22/2011 Smith & Nephew Inc
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