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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
510(K) Number: K120992
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Product Description
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Recall
Class
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FDA Recall
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Tibial Component Metal Cased Small Long; Tibial Component Metal Cased Small Short; Tibial Component ... 2 12/19/2016 Stanmore Implants Worldwide Ltd.
Tibial Component Fixed Hinge Small Long; Tibial Component Fixed Hinge Small Short The product is a ... 2 12/19/2016 Stanmore Implants Worldwide Ltd.
DF Coated Integral Shaft & Stem 15x30x38; DF Coated Integral Shaft & Stem 15x36x44; DF Coated ... 2 12/19/2016 Stanmore Implants Worldwide Ltd.
Femoral Shaft L=120mm; Femoral Shaft L=135mm; Femoral Shaft L=150mm The product is a component is a... 2 12/19/2016 Stanmore Implants Worldwide Ltd.
Femoral Integral Shaft & Stem 15x27 HA Coated; Femoral Integral Shaft & Stem 15x30 HA Coated; Fe... 2 12/19/2016 Stanmore Implants Worldwide Ltd.
METS SMILES Total Knee Replacement 2 08/17/2016 Stanmore Implants Worldwide Ltd.
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