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Class II: temporary or reversible health riskOngoing

Den-Mat Holdings Hydrogen Peroxide Oral Rinse Recall

Hydrogen Peroxide Oral Rinse, Significantly Reduces Bacteria, Fresh Mint Flavor, Alcoho…

Den-Mat Holdings, LLC · Lompoc, CA

Risk level
Class II
Reported by FDA
Feb 7, 2024
Recall ID
D-0287-2024
Check your lot numberHow we source this data

Summary

Den-Mat Holdings recalled Hydrogen Peroxide Oral Rinse starting Jan 16, 2024. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0287-2024 on Feb 7, 2024. Reason: CGMP Deviations: products may not conform to the labeled specifications. Status: Ongoing.

Why it was recalled

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

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.

Lot numbers, UPCs & expiration codes

Lot #: a) 2214500032, 2216700041, 2301900118, 2312600002, 2204800002, Exp. 02/05/2024; 2306100034, 2322000078, 2322200021 02/22/2024; 2318000026, Exp 02/24/2024; 2323000070, 2324400005, 2323300016, Exp 08/29/2025; 2324800079, Exp 08/30/2025; 2325800008, Exp 09/18/2025; 2328600011, 2328600032, 10/10/2025; 2324800123, Exp 10/11/2025; 2329700005, 2329700090, Exp 10/19/2025; 2330400003, Exp 10/25/2025; 2334100101, Exp 11/13/2025; 2335300019, 2335400038, Exp 12/19/2025. b) 2212200014, Exp 02/22/2024; 2323300017, Exp 08/29/2025; 2324800124, Exp 09/18/2025. c) 2211100001, Exp 02/24/2024; 2330500009, Exp 10/25/2025; 2333200014, Exp12/19/2025.

Where it was sold

Nationwide in the US

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0287-2024
Classification
Class II
Status
Ongoing
Recall initiated
Jan 16, 2024
FDA report date
Feb 7, 2024
Quantity
10,103 units
Recall type
Voluntary: Firm initiated
Recalling firm
Den-Mat Holdings, LLC

Original FDA data

Every field from FDA enforcement report D-0287-2024, exactly as published.

Show all FDA fields
City
Lompoc
State
CA
Status
Ongoing
Country
United States
Event ID
93831
Address
1017 W Central Ave
Code information
Lot #: a) 2214500032, 2216700041, 2301900118, 2312600002, 2204800002, Exp. 02/05/2024; 2306100034, 2322000078, 2322200021 02/22/2024; 2318000026, Exp 02/24/2024; 2323000070, 2324400005, 2323300016, Exp 08/29/2025; 2324800079, Exp 08/30/2025; 2325800008, Exp 09/18/2025; 2328600011, 2328600032, 10/10/2025; 2324800123, Exp 10/11/2025; 2329700005, 2329700090, Exp 10/19/2025; 2330400003, Exp 10/25/2025; 2334100101, Exp 11/13/2025; 2335300019, 2335400038, Exp 12/19/2025. b) 2212200014, Exp 02/22/2024; 2323300017, Exp 08/29/2025; 2324800124, Exp 09/18/2025. c) 2211100001, Exp 02/24/2024; 2330500009, Exp 10/25/2025; 2333200014, Exp12/19/2025.
Postal code
93436-2701
Report date
Feb 7, 2024
Product type
Drugs
Recall number
D-0287-2024
Classification
Class II
Recalling firm
Den-Mat Holdings, LLC
Product quantity
10,103 units
Reason for recall
CGMP Deviations: products may not conform to the labeled specifications.
Voluntary / mandated
Voluntary: Firm initiated
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.
Distribution pattern
Nationwide in the US
Recall initiation date
Jan 16, 2024
Initial firm notification
Letter
Center classification date
Jan 31, 2024

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0287-2024, published Feb 7, 2024. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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