FDA recall record

Den-Mat Holdings Hydrogen Peroxide Oral Rinse, Significantly Reduces Bacteria, Fresh Mint recall — FDA D-0287-2024

CGMP Deviations: products may not conform to the labeled specifications.

Class IIclassification
D-0287-2024official record ID
Feb 7, 2024report date

Recall record at a glance

Official recordD-0287-2024
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmDen-Mat Holdings, LLC
Report dateFeb 7, 2024
Recall initiation dateJan 16, 2024
Quantity10,103 units
LocationLompoc, CA, United States

Official product description

Hydrogen Peroxide Oral Rinse, Significantly Reduces Bacteria, Fresh Mint Flavor, Alcohol Free, a)16 fl. oz. (473 mL) bottle, NDC 59883-202-16, UPC 3 59883 00009 7); b) 64 fl. oz. (1.89 L) bottle, NDC 59883-202-64; c) 128 fl. oz. (1 gal) 3.78L bottle, NDC 59883-202-28, UPC 3 59883 00007 3), Manufactured by: Den-Mat Holdings, LLC, Lompoc, CA 93436.

Why the product was recalled

CGMP Deviations: products may not conform to the labeled specifications.

Distribution information

Nationwide in the US

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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.