Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-3016-2020 - KIT, PRE OP DRAH - Product Usage: Preoperative kit used to decolonize intranasal S. aureus. | 2 | 09/25/2020 |
FEI # 3002973487 Cardinal Health 200, LLC |
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