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Class II: temporary or reversible health riskTerminated

Colgate Palmolive hello wild strawberry fluoride toothpaste Recall

hello wild strawberry fluoride toothpaste, sodium fluoride 0

Colgate Palmolive Company · Piscataway, NJ

Risk level
Class II
Reported by FDA
Aug 23, 2023
Recall ID
D-1084-2023
Check your lot numberHow we source this data

Summary

Colgate Palmolive recalled hello wild strawberry fluoride toothpaste starting Aug 10, 2023. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1084-2023 on Aug 23, 2023. Reason: Labeling: Label Mix-Up: Some hello wild strawberry fluoride toothpaste, packaged in cartons labeled as hello wild strawberry fluoride toothpaste were incorrectly filled in tubes labeled as hello fresh watermelon fluoride free toothpaste. Status: Terminated.

Why it was recalled

Labeling: Label Mix-Up: Some hello wild strawberry fluoride toothpaste, packaged in cartons labeled as hello wild strawberry fluoride toothpaste were incorrectly filled in tubes labeled as hello fresh watermelon fluoride free toothpaste.

Product description

hello wild strawberry fluoride toothpaste, sodium fluoride 0.24% (0.15% w/v fluoride ion), NET WT 4.2 OZ (119 g), Distributed by Hello Products LLC, Montclair, NJ 07042, UPC 8 19156 02026 4 (carton), 12-count case GTIN: 20819156020268; strawberry tubes also sold in Strawberry 3-pack overwrap UPC 8 19156 02349 4, UPC 10819156023491 case; in the variety 3-pack of Strawberry + Unicorn + Grape UPC 8 19156 02332 6, UPC 10819156023323 case; and in a 24-count Toothpaste Floorstand, UPC 819156020684 (case).

Lot numbers, UPCs & expiration codes

Lot #: 004287, 2267USA94A, 2271USA94A, EXP 08/2024; 3053USA94A, Exp 01/2025; 3156USA94A, 3157USA94A, EXP 05/2025

Where it was sold

Nationwide in the USSA

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-1084-2023
Classification
Class II
Status
Terminated
Recall initiated
Aug 10, 2023
FDA report date
Aug 23, 2023
Quantity
182,046 tubes
Recall type
Voluntary: Firm initiated
Recalling firm
Colgate Palmolive Company

Original FDA data

Every field from FDA enforcement report D-1084-2023, exactly as published.

Show all FDA fields
City
Piscataway
State
NJ
Status
Terminated
Country
United States
Event ID
92835
Address
909 River Rd
Code information
Lot #: 004287, 2267USA94A, 2271USA94A, EXP 08/2024; 3053USA94A, Exp 01/2025; 3156USA94A, 3157USA94A, EXP 05/2025
Postal code
08854-5503
Report date
Aug 23, 2023
Product type
Drugs
Recall number
D-1084-2023
Classification
Class II
Recalling firm
Colgate Palmolive Company
Product quantity
182,046 tubes
Termination date
Apr 1, 2024
Reason for recall
Labeling: Label Mix-Up: Some hello wild strawberry fluoride toothpaste, packaged in cartons labeled as hello wild strawberry fluoride toothpaste were incorrectly filled in tubes labeled as hello fresh watermelon fluoride free toothpaste.
Voluntary / mandated
Voluntary: Firm initiated
Product description
hello wild strawberry fluoride toothpaste, sodium fluoride 0.24% (0.15% w/v fluoride ion), NET WT 4.2 OZ (119 g), Distributed by Hello Products LLC, Montclair, NJ 07042, UPC 8 19156 02026 4 (carton), 12-count case GTIN: 20819156020268; strawberry tubes also sold in Strawberry 3-pack overwrap UPC 8 19156 02349 4, UPC 10819156023491 case; in the variety 3-pack of Strawberry + Unicorn + Grape UPC 8 19156 02332 6, UPC 10819156023323 case; and in a 24-count Toothpaste Floorstand, UPC 819156020684 (case).
Distribution pattern
Nationwide in the USSA
Recall initiation date
Aug 10, 2023
Initial firm notification
Letter
Center classification date
Aug 14, 2023

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1084-2023, published Aug 23, 2023. View the source record (openFDA) · FDA enforcement reports

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

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