Medical Device Recalls
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21 to 21 of 21 Results
510(K) Number: K121822 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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American Surgical Delicot 30mm x 70mm Ref: 63-10 Product Usage: Neurosurgical and Nonneurosurgica... | 2 | 05/26/2016 | American Surgical Company |
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