Anabolic Research WINN-50 (vanazolol). Dietary Supplement. 90 Capsules. UPC 8 51840-00707 6. Manafactured For: Anab
Summary
The FDA issued a Class III for Anabolic Research WINN-50 (vanazolol). Dietary Supplement. 90 Capsules. UPC 8 by Dynamic Sports Nutrition. Reason: Dietary supplement involved degradation of an ingredient. Product is sub-potent for Vitamin B12 not meeting label claims..
Details
Source
Food Recall
External ID
H-0573-2025
Action Date
2025-09-17
Status
Terminated
Category
food
Product Description
Anabolic Research WINN-50 (vanazolol). Dietary Supplement. 90 Capsules. UPC 8 51840-00707 6. Manafactured For: Anabolic Research, 6942 FM 1960 E. #346, Humble, TX 77346-2706.
Lot/Code Info: LOT: 2307149 MFG: 07/2023
Quantity Affected: 1,566 bottles -2.4 oz each
Reason for Recall
Dietary supplement involved degradation of an ingredient. Product is sub-potent for Vitamin B12 not meeting label claims.
Distribution
Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2025-07-28
Company
Humble, TX
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 28 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Dynamic Sports Nutrition) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Dynamic Sports Nutrition have FDA actions?
This is the only FDA action we have on record for Dynamic Sports Nutrition in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0573-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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