Yes — there is an active recall. 112 ongoing FDA recalls mention Alcohol (458 total). Check the affected lots below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Alcohol. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed.
Reason CGMP Deviations: recalled because it was manufactured in the same facility as the product found to contain methanol which represents poor Current…
Reason CGMP Deviations: Products manufactured at the same site were FDA testing found below the label claim for ethanol content and the presence of…
Reason Non-sterility: Product is being recalled to climatic Zone IV regions of the world where at the labeled storage conditions of 30*C/75% Relative…
Reason Microbial Contamination of Non-Sterile Product: Product is being recalled to climatic Zone IV regions of the world where at the labeled storage…
Reason Microbial Contamination of Non-Sterile Products:Product is being recalled to climatic Zone IV regions of the world where at the labeled storage…
Reason Non-sterility: Product is being recalled to climatic Zone IV regions of the world where at the labeled storage conditions of 30*C/75% Relative…
Reason Chemical Contamination: Product contains methanol.
Reason CGMP Deviations
Reason Chemical Contamination: Presence of Undeclared Methanol
Reason CGMP Deviations: Product was found to be below the label claim for ethanol content and the presence of undeclared methanol.
Reason Chemical Contamination: Product contains undeclared methanol.
Reason Non-Sterility: Product is being recalled due to presence of Aspergillus Penicilloides
Reason Non-Sterility: Product is being recalled due to presence of Aspergillus Penicilloides
Reason Non-Sterility: Product is being recalled due to presence of Aspergillus Penicilloides
Reason Chemical Contamination: Product contains undeclared methanol.
Reason Subpotent Drug: active ingredient ethanol tested below label claim and there is presence of undeclared isopropyl alcohol.
Reason Subpotent Drug: active ingredient ethanol tested below label claim and there is presence of undeclared isopropyl alcohol.
Reason Subpotent Drug: active ingredient ethanol tested below label claim and there is presence of undeclared isopropyl alcohol.
Reason Incorrect/Undeclared Excipients: Notification received from Health Canada that DA-2I Ethanol is a type not an approved for use in Hand Sanitizer.
Reason Incorrect/Undeclared Excipients: Notification received from Health Canada that DA-2I Ethanol is a type not an approved for use in Hand Sanitizer.
Reason Subpotent Drug: Product was found to be subpotent. Product also has high pH levels
Reason Failed Impurities/Degradation Specifications: elevated levels of Benzaldehyde impurity was found in investigative samples (retain samples).
Reason CGMP Deviations: products were not manufactured under current good manufacturing practices.
Reason Presence of Foreign Substance; Fiber particles.
Reason Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small particles of an inert plastic material introduced during manufacturing.
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