CLASS II ONGOING Food recall · Reported 31 May 2023 · FDA Enforcement Report

TruControl 7 Day Trifold recalled by TruVision Health

TruVision Health is recalling TruControl 7 Day Trifold, distributed in 50 states. The recall was initiated on 27 Apr 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot WKW72353
Quantity recalledUnknown

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0941-2023
FDA event ID
92173
Recalling firm
TruVision Health, Draper, UT
Classification
Class II
Status
Ongoing
Recall initiated
27 Apr 2023
FDA classified
25 May 2023
Reported
31 May 2023
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Other Reasons
Product category
Other

Timeline

27 Apr 2023Recall initiated by company
25 May 2023Classified by FDA+28 days
31 May 2023Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

TruControl 7 Day Trifold

Where it was distributed

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

AlaskaAlabamaArkansasArizonaCaliforniaColoradoConnecticutDelawareFloridaGeorgiaHawaiiIowaIdahoIllinoisIndianaKansasKentuckyLouisianaMassachusettsMaryland

Questions about this recall

Is TruControl 7 Day Trifold recalled?

Yes. TruVision Health recalled TruControl 7 Day Trifold on 27 Apr 2023. The recall is Class II and its status is Ongoing. Recall number F-0941-2023.

Why was it recalled?

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

Which lots are affected?

Lot WKW72353

Where was it 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 should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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