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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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Z-0585-2022 - KWIK-STIK, Quality control kit for culture media, sold as: a. KWIK-STIK 2-pack Enterococcus faecalis derived from ATCC 51299 b. KWIK-STIK 6-pack Enterococcus faecalis derived from ATCC 51299 2 02/08/2022 FEI # 2150138
Microbiologics Inc
Z-0586-2022 - LYFO-DISK Enterococcus faecalis derived from ATCC 51299 In Vitro Diagnostic Control microorganisms 2 02/08/2022 FEI # 2150138
Microbiologics Inc
Z-0587-2022 - QC Sets and Panels, KWIK-STIK AST-GP (4 Strains) QC Set. KWIK-STIK kit that contains Catalog Number 0959P. In Vitro Diagnostic Control microorganisms 2 02/08/2022 FEI # 2150138
Microbiologics Inc
Z-0588-2022 - QC Sets and Panels, KWIK-STIK AST-GP (6 Strains) QC Set. KWIK-STIK kit that contains Catalog Number 0959P. In Vitro Diagnostic Control microorganisms 2 02/08/2022 FEI # 2150138
Microbiologics Inc
Z-0589-2022 - QC Sets and Panels, KWIK-STIK Blood Culture Identification (BCID) Verification Panel (Live Culture). KWIK-STIK kit that contains Catalog Number 0959P. In Vitro Diagnostic Control microorganisms 2 02/08/2022 FEI # 2150138
Microbiologics Inc
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