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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 2 of 2 Results
Related Medical Device Recalls Date Classified to: 10/25/2014
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Product Description
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Z-1544-2012 - PATIENT SPECIFIC INSTRUMENTS N-K FLEX PIN GUIDES (FEMUR AND TIBIA) NONSTERILE ~ MUST BE STERILIZED PRIOR TO USE Patient ID ..- 0864-R3 Manufactured by Materialise, Plymouth, MI Distributed by Zi... 2 May-14-2012 Materialise USA LLC
Z-1543-2012 - PATIENT SPECIFIC INSTRUMENTS LPS-FLEX PIN GUIDES (FEMUR AND TIBIA) NONSTERILE ~ MUST BE STERILIZED PRIOR TO USE Patient ID--0242-LF Manufactured by Materialise, Plymouth, MI Distributed by Zimm... 2 May-14-2012 Materialise USA LLC
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