Medical Device Recalls
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510(K) Number: K041021 |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| R-F Injector Cannula. 20gx10cm-STERILE. REF/UDI: 257-2010/(01)10818788022124; REF/UDI: 257-2010D(01)... | 2 | 04/16/2020 | Epimed International |
| R-F Injector Cannula. 18gx10cm-STERILE. REF/UDI: 257-1810/(01)00828788021496; REF/UDI: 257-1810D(01)... | 2 | 04/16/2020 | Epimed International |
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