Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Is Alcohol recalled?

Yes — there is an active recall. 119 ongoing FDA recalls mention Alcohol (464 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. Checked against openFDA on Oct 10, 2026.

Alcohol recalls on record

none so far in 2026; 464 on record, newest first
Class I · High risk

BD ChloraPrep Hi-Lite Orange 26 mL Applicator

Defective Delivery System: An increase in complaints identified endcap being loose or falling off upon activation releasing glass shards containing the solution.

Terminated Packaging defect CareFusion 213, LLC NDC 54365-400-38 D-0373-2021
Class II · Moderate risk

ChloraPrep With Tint 2% w/v chlorhexidine gluconate

CGMP Deviations: Product is being recalled because at labeled storage conditions of 30*C/75% Relative Humidity, there is the potential for growth of Aspergillus penicillioides, a type of fungus, resulting in a breach of the package integrity.

Terminated Labeling / mix-up CareFusion 213, LLC D-0350-2021
Class II · Moderate risk

ChloraPrep One-Step 2% w/v chlorhexidine gluconate

CGMP Deviations: Product is being recalled because at labeled storage conditions of 30*C/75% Relative Humidity, there is the potential for growth of Aspergillus penicillioides, a type of fungus, resulting in a breach of the package integrity.

Terminated Labeling / mix-up CareFusion 213, LLC D-0349-2021
Class II · Moderate risk

BD ChloraPrep Hi-Lite Orange 2% w/v chlorhexidine gluconate

Lack of Assurance of Sterility: Product is being recalled because at labeled storage conditions of 30*C/75% Relative Humidity, there is the potential for growth of Aspergillus penicillioides, a type of fungus, resulting in a breach of the package integrity.

Terminated Sterility / contamination CareFusion 213, LLC NDC 54365-400-33 D-0348-2021
Class II · Moderate risk

BD ChloraPrep Clear

Lack of Assurance of Sterility: Product is being recalled because at labeled storage conditions of 30*C/75% Relative Humidity, there is the potential for growth of Aspergillus penicillioides, a type of fungus, resulting in a breach of the package integrity.

Terminated Sterility / contamination CareFusion 213, LLC NDC 54365-400-32 D-0347-2021
Class I · High risk

ChloraPrep With Tint 2% w/v chlorhexidine gluconate

Microbial Contamination of Non-Sterile Product:.Product is being recalled because at labeled storage conditions of 30*C/75% Relative Humidity, growth of Aspergillus penicillioides, a type of fungus, resulted in a breach of the package integrity.

Terminated Microbial contamination CareFusion 213, LLC D-0346-2021
Class I · High risk

ChloraPrep One-Step 2% w/v chlorhexidine gluconate

Microbial Contamination of Non-Sterile Product.Product is being recalled because at labeled storage conditions of 30*C/75% Relative Humidity, growth of Aspergillus penicillioides, a type of fungus, resulted in a breach of the package integrity.

Terminated Microbial contamination CareFusion 213, LLC D-0345-2021
Class I · High risk

BD ChloraPrep Clear

Non-sterility.Product is being recalled because at labeled storage conditions of 30*C/75% Relative Humidity, growth of Aspergillus penicillioides, a type of fungus, resulted in a breach of the package integrity.

Terminated Sterility / contamination CareFusion 213, LLC NDC 54365-400-32 D-0343-2021
Class II · Moderate risk

Ferrous Sulfate 75 mg

CGMP Deviations: Intermittent exposure to temperature excursion during storage.

Terminated Temperature excursion Cardinal Health Inc. NDC 54838-011-50 D-0504-2021
Class II · Moderate risk

Durisan Antimicrobial Solutions

CGMP Deviations: lots recalled due to CGMP deviations because they were manufactured under the same conditions as product lots found to be contaminated.

Terminated cGMP deviation Sanit Technologies, LLC dba Durisan D-0658-2021
Class I · High risk

Durisan Antimicrobial Solutions

Microbial Contamination of Non-Sterile Products: firm's internal testing found certain lots of the product to be contaminated with Burkholderia contaminans and/or yeast and mold.

Terminated Microbial contamination Sanit Technologies, LLC dba Durisan D-0656-2021
Class I · High risk

heal the world

Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers resembling drinking water bottles.

Terminated Labeling / mix-up Pnhc, LLC. D-0365-2021
Class II · Moderate risk

Paroex (Chlorhexidine Gluconate)

cGMP Deviations; FDA inspection of manufacturing facility observed potential Burkholderia cepacia complex (BCC) contamination, inadequate cleaning, inadequate microbiological testing, and insanitary conditions

Ongoing Microbial contamination Sunstar Americas, Inc. NDC 52376-021-02 D-0222-2021
Class II · Moderate risk

IMC Wash-Free Hand Sanitizer

CGMP Deviations: product manufactured at the same facility that produced product that FDA sampled and found to be subpotent for ethanol and contained methanol.

Terminated Chemical / undeclared Shane Erickson Inc D-0241-2021
Class II · Moderate risk

IMC Wash-Free Hand Sanitizer

CGMP Deviations: product manufactured at the same facility that produced product that FDA sampled and found to be subpotent for ethanol and contained methanol.

Terminated Chemical / undeclared Shane Erickson Inc D-0240-2021
Class II · Moderate risk

IMC Wash-Free Hand Sanitizer

CGMP Deviations: product manufactured at the same facility that produced product that FDA sampled and found to be subpotent for ethanol and contained methanol.

Terminated Chemical / undeclared Shane Erickson Inc D-0239-2021