Medical Device Recalls
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1 result found
510(K) Number: K150874 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Dial-A-Dose Insulin Delivery Device (Pen-Injector) cartridge holders Product Usage: The NovoPen ... | 2 | 12/07/2017 | Novo Nordisk Inc |
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