Medical Device Recalls
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1 to 8 of 8 Results
510(K) Number: K161273 |
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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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BIOMET StageOne Knee Femoral Cement Spacer Mold, 60 MM, Silicone, Sterile, Item 432160. | 2 | 04/03/2020 | Biomet, Inc. |
BIOMET StageOne Knee Femoral Cement Spacer Mold, 65 MM, Silicone, Sterile, Item 432165. | 2 | 04/03/2020 | Biomet, Inc. |
BIOMET StageOne Knee Femoral Cement Spacer Mold, 70 MM, Silicone, Sterile, Item 432170. | 2 | 04/03/2020 | Biomet, Inc. |
BIOMET StageOne Knee Tibial Cement Spacer Mold, 80 MM, Silicone, Sterile, Item 433180. | 2 | 04/03/2020 | Biomet, Inc. |
BIOMET StageOne Knee Tibial Cement Spacer Mold, 65 MM, Silicone, Sterile, Item 433165. | 2 | 04/03/2020 | Biomet, Inc. |
BIOMET StageOne Knee Tibial Cement Spacer Mold, 70 MM, Silicone, Sterile, Item 433170. | 2 | 04/03/2020 | Biomet, Inc. |
BIOMET StageOne Knee Tibial Cement Spacer Mold, 75 MM, Silicone, Sterile, Item 433175. | 2 | 04/03/2020 | Biomet, Inc. |
BIOMET StageOne Knee Femoral Cement Spacer Mold, 75 MM, Silicone, Sterile, Item 432175. | 2 | 04/03/2020 | Biomet, Inc. |
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