Medical Device Recalls
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1 result found
Recall Number: Z-0876-2026 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, C... | 2 | 12/02/2025 |
FEI # 2150138 Microbiologics Inc |
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