Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K052990 |
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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, Hip Cement Spacer Mold w/Reinforcement, 9 X 125 MM, 51 MM, Silicone, Sterile, Item ... | 2 | 04/03/2020 | Biomet, Inc. |
BIOMET StageOne, Hip Cement Spacer Mold w/Reinforcement, 9 X 125 MM, 43 MM, Silicone, Sterile, Item ... | 2 | 04/03/2020 | Biomet, Inc. |
BIOMET StageOne, Hip Cement Spacer Mold w/Reinforcement, 17 X 165 MM, 64 MM, Silicone, Sterile, Item... | 2 | 04/03/2020 | Biomet, Inc. |
BIOMET StageOne, Hip Cement Spacer Mold w/Reinforcement, 13 X 145 MM, 57 MM, Silicone, Sterile, Item... | 2 | 04/03/2020 | Biomet, Inc. |
StageOne Hip, Models 431207 & 431209Usage: Product Usage: The single-use cement spacer molds a... | 2 | 11/07/2018 | Zimmer Biomet, Inc. |
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