Medical Device Recalls
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11 to 13 of 13 Results
510(K) Number: K083566 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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R3 (TM) 22 MM I.D., 54 MM O.D., CONSTRAINED LINER, UHMWPE, CO-CR, TI-6AL-4V, REF 71339154, STERILE E... | 2 | 10/18/2010 | Smith & Nephew Inc |
R3 (TM) 22 MM I.D., 52 MM O.D., CONSTRAINED LINER, UHMWPE, CO-CR, TI-6AL-4V, REF 71339152, STERILE E... | 2 | 10/18/2010 | Smith & Nephew Inc |
R3 (TM) 28 MM I.D., 64 MM O.D., CONSTRAINED LINER, UHMWPE, CO-CR, TI-6AL-4V, REF 71339164, STERILE E... | 2 | 10/18/2010 | Smith & Nephew Inc |
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