Lower riskFood recall · FDA · Published July 13, 2020
Lopez Gonzalez Santana BTREX PLUS Dietary Supplement Recall: Damaged Tablets
Lopez Gonzalez Santana recalls BTREX PLUS dietary supplement 2 caplets (UPC 05380930802) due to damaged tablets in physician samples. Consumers should check lot numbers 32179 (exp 9/2022) and 33278 (exp 12/2022).
“Lopez Gonzalez Santana BTREX PLUS Dietary Supplement Recall: Damaged Tablets.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/15506-lopez-gonzalez-santana-btrex-plus-dietary-supplement-recall-damaged-tablets. Based on FDA recall #F-0540-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0540-2021%22&limit=1).
The FDA announced on July 13, 2020, that Lopez Gonzalez Santana Corporation voluntarily recalled BTREX PLUS Dietary Supplement 2 Caplets due to cGMP deviations involving damaged tablets. The recall affects physician samples distributed in Puerto Rico.
How to tell if you have it
BTREX PLUS, Dietary Supplement 2 Caplets
UPC 05380930802 (Physician Samples)
Lot #32179, Exp. 9/2022
Lot #33278, Exp. 12/2022
The hazard
The recall is due to cGMP deviations resulting in the presence of damaged tablets within the product.
Context
GovInfoNow's records show Lopez Gonzalez Santana Corporation has two other recalls on record since April 20, 2021. Other recent recalls of similar products include Llorens Vitamin B-Complex Supplement Recall (May 7, 2026), Wellnov Liposomal Mens 50+ Liquid Multivitamin Drops Recall (April 23, 2026), and Aonic Complete His. Dosage Liquid Supplement Recall (January 15, 2026).
How to tell if you have this one
Check the UPC 05380930802 label on the product. Look for lot numbers 32179 (expiring 9/2022) or 33278 (expiring 12/2022) on the packaging.
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-0540-2021 (July 13, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0540-2021 to see it in context.
Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
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