Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K032295 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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GENESIS(R) II, POSTERIOR STABILIZED ARTICULAR INSERT, SIZE 1-2, 13 MM QTY: (1), REF 71420806, STERIL... | 2 | 12/04/2013 | Smith & Nephew Inc |
GENESIS(R) II, PS HIGH FLEXION ARTICULAR INSERT, SIZE 3-4, 13 MM QTY: (1), REF 71420820, STERILE EO... | 2 | 12/04/2013 | Smith & Nephew Inc |
GENESIS(R) II, MOBILE BEARING ARTICULAR INSERT RIGHT, SIZE 5, 9 MM QTY: (1), REF 71621509, STERILE E... | 2 | 12/04/2013 | Smith & Nephew Inc |
GENESIS(R) II, PS HIGH FLEXION ARTICULAR INSERT, SIZE 5-6, 9 MM QTY: (1), REF 71421515, STERILE EO... | 2 | 12/04/2013 | Smith & Nephew Inc |
GENESIS(R) II, PS HIGH FLEXION ARTICULAR INSERT, SIZE 5-6, 11 MM QTY: (1), REF 71421516, STERILE EO,... | 2 | 12/04/2013 | Smith & Nephew Inc |
GENESIS(R) II, PS HIGH FLEXION ARTICULAR INSERT, SIZE 3-4, 9 MM QTY: (1), REF 71421508, STERILE EO... | 2 | 12/04/2013 | Smith & Nephew Inc |
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