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Class II: temporary or reversible health riskOngoing

TruVision Health TruBoost Drink Recall

TruBoost Drink - Ruby Rev

TruVision Health LLC · Draper, UT

Risk level
Class II
Reported by FDA
May 31, 2023
Recall ID
F-0951-2023
Check your lot numberHow we source this data

Summary

TruVision Health recalled TruBoost Drink starting Apr 27, 2023. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0951-2023 on May 31, 2023. Reason: The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients. Status: Ongoing.

Why it was recalled

The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

Product description

TruBoost Drink - Ruby Rev

Lot numbers, UPCs & expiration codes

Lot PM18821F1

Where it was sold

Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming and Australia, Canada, England, Germany, Ireland, New Zealand

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0951-2023
Classification
Class II
Status
Ongoing
Recall initiated
Apr 27, 2023
FDA report date
May 31, 2023
Quantity
4,650 packs
Recall type
Voluntary: Firm initiated
Recalling firm
TruVision Health LLC

Original FDA data

Every field from FDA enforcement report F-0951-2023, exactly as published.

Show all FDA fields
City
Draper
State
UT
Status
Ongoing
Country
United States
Event ID
92173
Address
172 E 14075 S
Code information
Lot PM18821F1
Postal code
84020-5725
Report date
May 31, 2023
Product type
Food
Recall number
F-0951-2023
Classification
Class II
Recalling firm
TruVision Health LLC
Product quantity
4,650 packs
Reason for recall
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Voluntary / mandated
Voluntary: Firm initiated
Product description
TruBoost Drink - Ruby Rev
Distribution pattern
Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming and Australia, Canada, England, Germany, Ireland, New Zealand
Recall initiation date
Apr 27, 2023
Initial firm notification
Press Release
Center classification date
May 25, 2023

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0951-2023, published May 31, 2023. View the source record (openFDA) · FDA enforcement reports

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

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