Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K031280 |
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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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Ultra-Drive Hose/Drape Assembly, Reference Number 423833 - Product Usage: Item used with the UltraDr... | 2 | 07/12/2019 | Zimmer Biomet, Inc. |
Ultra-Drive Irrigation Tubing Assembly, Reference Number 423834 - Product Usage: Item used with the ... | 2 | 07/12/2019 | Zimmer Biomet, Inc. |
Ultra-DriveTool, 6 MM Plug Puller, REF 423868. Recommended Power Setting 70 For Single Use Only, Ste... | 3 | 05/10/2012 | Biomet, Inc. |
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