There is a possibility of reproducibility, accuracy, and/or QC failures in antibiotic susceptibility testing (AST) for H. influenzae. This may cause product discard, delayed results, or additional adverse diagnostic outcomes, such as a delay in diagnosis, the selection of inappropriate antibiotics, or extended duration of antibiotic exposure and the treatment process.
Reason for recall: There is a possibility of reproducibility, accuracy, and/or QC failures in antibiotic susceptibility testing (AST) for H. influenzae. This may cause product discard, delayed results, or additional adverse diagnostic outcomes, such as a delay in diagnosis, the selection of inappropriate antibiotics, or extended duration of antibiotic exposure and the treatment process. Distribution: Domestic distribution nationwide. International distribution worldwide. Quantity: 2,363,168 total units Lot/code info: Catalog No. 231691 UDI-DI 00382902316916 Lots 1301719 2026369 2056587 2119595 3003951 3062107 3118199 3275730; Catalog No. 231692¿ UDI-DI 30382902316924 Lots 3003951 3184117 3223408 3275730 1301719 2026369 2056587 2119595 2147716 2244463 3062107 3118199
00382902316916, 30382902316924
Official record: FDA (Device enforcement) ↗
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