Severity
Low
LowClass IIITerminated
FDA Food recall · Reported March 4, 2020
Lifetime Fitness D. Tox Shake Mix; Plant-Based Protein Blend. Dietary Supplement - Net Wt. 2.36 lb. (37.76 oz.) 1.07 kg Program Kit - Natural Vanilla Flavor UPC: 6 82471 00831-2 Product number: 6142-2646 Manufactured exclusively for: Life Time Fitness Inc. 2902 Corporate Place Chanhassan, MN 55317
Notified by supplier that flax seed used in products is under recall due to detection of unapproved herbicide.
The recall
Pro-Form Manufacturing LLC issued this low-severity FDA Food recall — Notified by supplier that flax seed used in products is under recall due to detection of unapproved herbicide..
- Low
- severity level
- 3K units
- affected scope
- Class III
- classification
- March 4, 2020
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0783-2020 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-0783-2020) was formally reported on March 4, 2020, with the manufacturer initiating the action on February 19, 2020. It is classified under Low severity (Class III), with a current status of Terminated. Pro-Form Manufacturing LLC is listed as the recalling firm, operating out of Benicia, CA. Federal records list the affected scope as 3,246 units.
The documented reason for this recall is: Notified by supplier that flax seed used in products is under recall due to detection of unapproved herbicide. Distribution data in the federal record shows the product reached: UT, MN. Some product was further distributed to Columbia, Mexico, Russia and Ukraine.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls — clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Outdoor & Sports recalls over time
Where this recall sits in its category — 321 outdoor & sports recalls on record
Where this recall sits in the database
Of 83,949 recalls in the database, 21,198 are high severity, 58,883 moderate, and 3,868 low. This recall is classified low severity.
Affected scope
3,246 units
Related Recalls
6
0 from same agency
Product description
Lifetime Fitness D. Tox Shake Mix; Plant-Based Protein Blend. Dietary Supplement - Net Wt. 2.36 lb. (37.76 oz.) 1.07 kg Program Kit - Natural Vanilla Flavor UPC: 6 82471 00831-2 Product number: 6142-2646 Manufactured exclusively for: Life Time Fitness Inc. 2902 Corporate Place Chanhassan, MN 55317
Reason for recall
Notified by supplier that flax seed used in products is under recall due to detection of unapproved herbicide.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | F-0783-2020 |
| Date reported | March 4, 2020 |
| Date initiated | February 19, 2020 |
| Recalling firm | Pro-Form Manufacturing LLC |
| Firm location | Benicia, CA |
| Affected scope | 3,246 units |
| Distribution | UT, MN. Some product was further distributed to Columbia, Mexico, Russia and Ukraine. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
Frequently Asked Questions
What product was recalled? ▼
Lifetime Fitness D. Tox Shake Mix; Plant-Based Protein Blend. Dietary Supplement - Net Wt. 2.36 lb. (37.76 oz.) 1.07 kg Program Kit - Natural Vanilla Flavor UPC: 6 82471 00831-2 Product number: 6142-2646 Manufactured exclusively for: Life Time Fitness Inc. 2902 Corporate Place Chanhassan, MN 55317. Recalled by Pro-Form Manufacturing LLC. Units affected: 3,246 units.
Why was this product recalled? ▼
Notified by supplier that flax seed used in products is under recall due to detection of unapproved herbicide.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on March 4, 2020. Severity: Low. Recall number: F-0783-2020.
Where was the recalled product distributed? ▼
Distribution: UT, MN. Some product was further distributed to Columbia, Mexico, Russia and Ukraine..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0783-2020) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported March 4, 2020.
- Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Read our methodology — how this data is sourced, computed, and verified.
Source: Federal recall agencies (FDA, CPSC, NHTSA) Aggregated federal recall feeds Recall data normalized across FDA, CPSC and NHTSA feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type).