FDA recall record

NCH Life Sciences Alcohol Antiseptic 80% Topical Solution Hand Sanitizer, Non-Sterile recall — FDA D-0092-2023

CGMP Deviations: Impurities of acetal and acetaldehyde were discovered in the product in excess of allowed limits.

Class IIclassification
D-0092-2023official record ID
Jan 4, 2023report date

Recall record at a glance

Official recordD-0092-2023
CategoryDrug Recalls
ClassificationClass II
FDA record statusCompleted
Recalling firmNCH Life Sciences LLC
Report dateJan 4, 2023
Recall initiation dateDec 9, 2022
Quantity10,930 gallons
LocationIrving, TX, United States

Official product description

Alcohol Antiseptic 80% Topical Solution Hand Sanitizer, Non-Sterile Solution, packaged as a a) 2.5 gallon bottle (9,464 ml), NDC 55533-524-02, and b) 55 gallon bottle (208,198 ml), NDC 55533-524-03, Manufactured for: Multi-Mist Products A Division of NCH Corporation 1618 Northgate, Irving, Texas 75062

Why the product was recalled

CGMP Deviations: Impurities of acetal and acetaldehyde were discovered in the product in excess of allowed limits.

Distribution information

Nationwide in United States and Canada.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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