Medical Device Recalls
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1 result found
510(K) Number: K101359 |
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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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Monoject 3mL Syringe with Hypodermic Safety Needle, 22G x 1-1/2 . Item Code 11832215 - Product Usage... | 2 | 03/09/2020 | Cardinal Health 200, LLC |
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