QiYu Hand Sanitizer (ethyl alcohol 75% (v/v)), 16.9 FL OZ (500 ML) bottles, Manufactured by: Guangzhou Minghui Cosmetics Co…
Reason Subpotent
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 Subpotent
Reason CGMP Deviations: Does not meet monograph for denaturant.
Reason CGMP Deviations: Does not meet monograph for denaturant.
Reason Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers resembling drinking water bottles.
Reason Subpotent
Reason Hand sanitizer packaged in bottles that resemble beverage containers.
Reason CGMP Deviations: lots and products of hand sanitizer are being recalled because they were manufactured under the same conditions as the product lot…
Reason CGMP Deviations: lots and products of hand sanitizer are being recalled because they were manufactured under the same conditions as the product lot…
Reason Chemical Contamination: FDA analysis found 1 lot of MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA (ethyl alcohol 70%) to be below the…
Reason Chemical Contamination: FDA analysis found 1 lot of MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA (ethyl alcohol 70%) to be below the…
Reason CGMP Deviations: lots and products of hand sanitizer are being recalled because they were manufactured under the same conditions as the product lot…
Reason CGMP Deviations: lots and products of hand sanitizer are being recalled because they were manufactured under the same conditions as the product lot…
Reason CGMP Deviations: Other lots and products of hand sanitizer recalled because they were manufactured under the same conditions as the product lots…
Reason CGMP Deviations: Other lots and products of hand sanitizer recalled because they were manufactured under the same conditions as the product lots…
Reason CGMP Deviations: Other lots and products of hand sanitizer recalled because they were manufactured under the same conditions as the product lots…
Reason Chemical Contamination: FDA analysis found 3 lots of DiBAR hand Sanitizer to be below the label claim for ethanol content and to contain methanol.
Reason Chemical contamination: product found to be contaminated with methanol (wood alcohol), benzene and acetaldehyde.
Reason Chemical contamination: product found to be contaminated with methanol (wood alcohol), benzene and acetaldehyde.
Reason Chemical contamination: product found to be contaminated with methanol (wood alcohol), benzene and acetaldehyde.
Reason Chemical contamination: product found to be contaminated with methanol (wood alcohol), benzene and acetaldehyde.
Reason Chemical contamination: product found to be contaminated with methanol (wood alcohol), benzene and acetaldehyde.
Reason Chemical contamination: product found to be contaminated with methanol (wood alcohol), benzene and acetaldehyde.
Reason Defective Delivery System: An increase in complaints identified endcap being loose or falling off upon activation releasing glass shards containing…
Reason CGMP Deviations: Product is being recalled because at labeled storage conditions of 30*C/75% Relative Humidity, there is the potential for growth of…
Reason CGMP Deviations: Product is being recalled because at labeled storage conditions of 30*C/75% Relative Humidity, there is the potential for growth of…
Tell us which medications you take. If the FDA recalls one, we email you - in plain English, with what to do. Free.