FDA recall record

HLI dba Humphreyline Alcohol-Free Hand Sanitizer, 1. fl. oz. (30 ml) bottles capped with recall — FDA D-1518-2014

Microbial Contamination of Non-Sterile Product

Class IIclassification
D-1518-2014official record ID
Aug 13, 2014report date

Recall record at a glance

Official recordD-1518-2014
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmHLI dba Humphreyline Inc.
Report dateAug 13, 2014
Recall initiation dateAug 6, 2014
Quantity975 bottles
LocationFlorence, KY, United States

Official product description

Alcohol-Free Hand Sanitizer, 1. fl. oz. (30 ml) bottles capped with white sprayer, OTC, contains Benzalkonium chloride. Mfg. for HLI, Portland, OR 97222 NDC: 19392-120-03. Labeled A) Anne Arundel County Mental Health Agency, Inc., B) Family Advocacy Program, and C) Henderson Community College Nursing.

Why the product was recalled

Microbial Contamination of Non-Sterile Product

Distribution information

Kentucky, Maryland, and Virginia.

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: Letter.

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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