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-2342-2018 - Safety Sideport Knife 1.0mm 45®, REF 378210 Product Usage: Indicated to make stab incisions during ophthalmic surgery | 2 | 07/02/2018 |
FEI # 1211998 Beaver Visitec |
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