[CORRECT FRONT PANEL] Hydrogen Peroxide Topical Solution, USP, 32 FL OZ (1 QT) 946 mL per bottle, NDC 0869-0871-45; [INCORRECT…
Reason Labeling; Label Mixup; some bottles have an incorrect back label indicating 91% Isopropyl Alcohol
458 FDA recalls mention Alcohol. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Alcohol.
Reason Labeling; Label Mixup; some bottles have an incorrect back label indicating 91% Isopropyl Alcohol
Reason Subpotent Drug
Reason Subpotent Drug
Reason Non-Sterility: contamination of Aspergillus penicillioides, due to breach in package lidding.
Reason Lack of assurance of sterility and cGMP deviations observed at the manufacturing site.
Reason LABELING: LABEL MIX-UP
Reason CGMP deviations
Reason Superpotent Drug
Reason CGMP Deviations: sterile water not used for production
Reason CGMP Deviations: sterile water not used for production
Reason CGMP deviations
Reason Chemical Contamination: Product manufactured with ethanol API that contains methanol
Reason Chemical Contamination: Product manufactured with ethanol API that contains methanol
Reason CGMP Deviations: products may not conform to the labeled specifications.
Reason CGMP Deviations: products may not conform to the labeled specifications.
Reason CGMP Deviations: Firm reported possible microbial contamination in the purified water used in the manufacturing of the products. No contamination was…
Reason Non-Sterility
Reason Non-Sterility
Reason Non-Sterility
Reason Non-Sterility
Reason OOS for viscosity
Reason Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility.
Reason Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility.
Reason Sub Potent and Super Potent Product: During an impact assessment of the DOP Hand Sanitizer product, it was identified that several lots distributed…
Reason Sub Potent and Super Potent Product: During an impact assessment of the DOP Hand Sanitizer product, it was identified that several lots distributed…
Tell us which medications you take. If the FDA recalls one, we email you - in plain English, with what to do. Free.