Medical Device Recalls
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41 to 44 of 44 Results
Related Medical Device Recalls |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Z-0964-2010 - JOURNEY " UNI TIBIAL INSERT RIGHT MEDIAL/ LEFT LATERAL, A/P 52 MM, M/L 30 MM, REF 71933302, QTY: (1), STERILE EO, SMITH & NEPHEW, INC. MEMPHIS, TN 38116 | 2 | 03/03/2010 | Smith & Nephew Inc |
Z-0965-2010 - JOURNEY " UNI TIBIAL INSERT RIGHT MEDIAL/ LEFT LATERAL, A/P 52 MM, M/L 30 MM, REF 71933303, QTY: (1), STERILE EO, SMITH & NEPHEW, INC. MEMPHIS, TN 38116 | 2 | 03/03/2010 | Smith & Nephew Inc |
Z-0966-2010 - JOURNEY " UNI TIBIAL BASEPLATE RIGHT MEDIAL/ LEFT LATERAL, A/P 38 MM, M/L 24 MM, REF 71422231, FOR CEMENTED USE ONLY, QTY: (1), STERILE R, SMITH & NEPHEW, INC. MEMPHIS, TN 38116 | 2 | 03/03/2010 | Smith & Nephew Inc |
Z-0925-2010 - JOURNEY " UNI TIBIAL BASEPLATE, LEFT MEDIAL/RIGHT LATERAL, A/P 42 MM, M/L 25 MM, REF 71422222, FOR CEMENTED USE ONLY, QTY: (1), STERILE R, SMITH & NEPHEW, INC. MEMPHIS, TN 38116 | 2 | 03/03/2010 | Smith & Nephew Inc |
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