Check the Batch
Class IIITerminated in FDA datasetRecall initiated Feb 19, 2020

Lifetime Fitness D. Tox Shake Mix; Plant-Based Protein Blend. Dietary Supplement - Net Wt. 2.50…

Recalling firm: Pro-Form Manufacturing LLC

Why it was recalled

Notified by supplier that flax seed used in products is under recall due to detection of unapproved herbicide.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 21, 2022.

Check your package

Compare the exact product and package details with the label you have.

ProductLifetime Fitness D. Tox Shake Mix; Plant-Based Protein Blend. Dietary Supplement - Net Wt. 2.50 lb. (40 oz.) 1.13 kg One gallon White HDPE Jar Natural Chocolate Flavor UPC: 6 82471 00830-5 Product number: 6142-2644 Manufactured exclusively for: Life Time Fitness Inc. 2902 Corporate Place Chanhassan, MN 55317
Package size2.50 lb
UPC682471008305

FDA code information

Lot Number: Kit Lot 20014-13 - Unit Lot 20014-11

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Full FDA record and distribution details

Original product description

Lifetime Fitness D. Tox Shake Mix; Plant-Based Protein Blend. Dietary Supplement - Net Wt. 2.50 lb. (40 oz.) 1.13 kg One gallon White HDPE Jar Natural Chocolate Flavor UPC: 6 82471 00830-5 Product number: 6142-2644 Manufactured exclusively for: Life Time Fitness Inc. 2902 Corporate Place Chanhassan, MN 55317

Extracted codes and context

TypeCode / valueContext
UPC682471008305. (40 oz.) 1.13 kg One gallon White HDPE Jar Natural Chocolate Flavor UPC: 6 82471 00830-5 Product number: 6142-2644 Manufactured exclusively for: Life Time Fitness Inc. 2902 Corporate Place Chanhassan,

Original FDA recall reason

Notified by supplier that flax seed used in products is under recall due to detection of unapproved herbicide.

Recall details

Recall number
F-0784-2020
Event ID
85063
FDA status
Terminated
Initiated
Feb 19, 2020
Reported
Mar 4, 2020
Classified
Mar 3, 2020
Terminated
Mar 21, 2022
Quantity
5,093 units
Location
Benicia, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

UT, MN. Some product was further distributed to Columbia, Mexico, Russia and Ukraine.

FDA source record · F-0784-2020

Data updated September 16, 2026. View official FDA data ↗

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