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

Polyvinyl Alcohol 1.4% Lubricating Eye Drops

Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility.

Terminated Sterility / contamination The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories NDC 0536-1325-94 D-0107-2024
Class II · Moderate risk

Equate Hand Sanitizer

Sub Potent and Super Potent Product: During an impact assessment of the DOP Hand Sanitizer product, it was identified that several lots distributed did not comply with the finished good acceptance criteria established.

Ongoing Wrong potency / content Omega & Delta Co., Inc. D-0105-2024
Class II · Moderate risk

DOP Instant Hand Sanitizer

Sub Potent and Super Potent Product: During an impact assessment of the DOP Hand Sanitizer product, it was identified that several lots distributed did not comply with the finished good acceptance criteria established.

Ongoing Wrong potency / content Omega & Delta Co., Inc. D-0104-2024
Class II · Moderate risk

DOP Instant Hand Sanitizer

Sub Potent and Super Potent Product: During an impact assessment of the DOP Hand Sanitizer product, it was identified that several lots distributed did not comply with the finished good acceptance criteria established.

Ongoing Wrong potency / content Omega & Delta Co., Inc. D-0103-2024
Class II · Moderate risk

Integrity Biochem HSC 70-VA

CGMP Deviation: Third party test results showing a presence of acetal and acetaldehyde at levels above USP specified amounts.

Terminated cGMP deviation Integrity Bio-Chemicals LLC D-0111-2024
Class II · Moderate risk

Integrity Biochem HSC70-LV

CGMP Deviation: Third party test results showing a presence of acetal and acetaldehyde at levels above USP specified amounts.

Terminated cGMP deviation Integrity Bio-Chemicals LLC D-0110-2024
Class II · Moderate risk

Integrity Biochem HSC 70-LM

CGMP Deviation: Third party test results showing a presence of acetal and acetaldehyde at levels above USP specified amounts.

Terminated cGMP deviation Integrity Bio-Chemicals LLC D-0109-2024
Class II · Moderate risk

BD ChloraPrep Clear

Stability data does not support expiry: Shelf-life of the impacted lots of BD ChloraPrep" Clear 1 mL Applicator cannot be substantiated beyond 12-months although labeled with 36-month expiry. Stability studies indicate that the impacted lots, if stored at 30¿C/75% relative humidity continuously beyond 12 months, may exhibit growth of Aspergillus penicillioides.

Completed Stability / shelf life CareFusion 213, LLC NDC 54365-400-31 D-1168-2023
Class II · Moderate risk

Foaming Hand Sanitizer

CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.

Terminated cGMP deviation Alpha Aromatics D-0760-2023
Class I · High risk

G-Supress DX

Product mix-up: incorrect product was found inside the G-Supress DX product carton.

Terminated Labeling / mix-up Novis PR, LLC dba Kramer Novis NDC 52083-655-01 D-0868-2023
Class II · Moderate risk

Isopropyl Alcohol Antiseptic 75%

CGMP deficiencies: Product manufactured at the same site where FDA testing found Presence of methanol in other products.

Terminated Chemical / undeclared Jarman's Midwest Cleaning Systems, Inc. D-0872-2023
Class II · Moderate risk

NaturalCare

CGMP Deviations: Raw material recalled by repackager, due to discoloration.

Ongoing Failed specification Nutraceutical Corporation D-0440-2023
Class II · Moderate risk

NaturalCare bioAllers

CGMP Deviations: Raw material recalled by repackager, due to discoloration.

Ongoing Failed specification Nutraceutical Corporation D-0439-2023