Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K932425 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Encore Medical Foundation Knee Revision Baseplate, Part Number 321-01-106, Size 6, Left | 2 | 02/24/2010 |
FEI # 1000116912 Encore Medical, Lp |
| Foundation Tibia Baseplate, Catalog number 324-01-108. The tibial is modular in design, such that p... | 2 | 01/13/2010 |
FEI # 1000116912 Encore Medical, Lp |
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