Medical Device Recalls
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1 to 2 of 2 Results
Related Medical Device Recalls Recall Date to: 09/21/2014 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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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 | 05/14/2012 | Materialise USA LLC |
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 | 05/14/2012 | Materialise USA LLC |
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