📍Recalling firmLopez Gonzalez Santana CorporationCalle De Diego # 488 Altos · Rio Piedras, PR 00924
✎ GovInfoNow plain-language explainer
Lopez Gonzalez Santana Corporation is recalling BTREX PLUS, a dietary supplement sold in 100-caplet bottles. The recall addresses current Good Manufacturing Practice (cGMP) deviations that resulted in the presence of damaged tablets within the product. This specific issue affects Lot #33277 with an expiration date of 12/22. Read more at govinfonow.com/recall/14678-btrex-plus-recall-damaged-tablets-in-dietary-supplement.
“BTREX PLUS Recall: Damaged Tablets in Dietary Supplement.” GovInfoNow, updated October 10, 2026. https://govinfonow.com/recall/14678-btrex-plus-recall-damaged-tablets-in-dietary-supplement. Based on FDA recall #F-0484-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0484-2021%22&limit=1).
The FDA announced on April 20, 2021, that Lopez Gonzalez Santana Corporation is recalling BTREX PLUS Dietary Supplement 100 Caplets due to cGMP deviations involving damaged tablets. The agency classified the recall as Class III.
How to tell if you have it
Brand: BTREX PLUS
Product: BTREX PLUS Dietary Supplement 100 Caplets
Lot #: 33277
Expiration date: 12/22
Quantity: 311 Bottles
The hazard
The recall addresses cGMP deviations related to the presence of damaged tablets in the product. The FDA classified this as a Class III recall.
Context
GovInfoNow's records show Lopez Gonzalez Santana Corporation has two other recalls on record since July 13, 2020. Other recent recalls of similar products include Blackseed Bitters 16oz/32oz Recall (April 6, 2026), Llorens Vitamin B-Complex Supplement Recall (May 7, 2026), and Liquid Blenz Soursop Bitters 16/32oz Recall (April 6, 2026).
How to tell if you have this one
Check your bottle for the brand name BTREX PLUS, Dietary Supplement 100 Caplets. Verify that the lot number is 33277 and the expiration date is 12/22.
Brand
BTREX PLUS
Category
Food
Where it went and when
Where it was distributed
Distributed in Puerto Rico.
Listed by the agency
Not listed
FDA distribution: “Domestic distribution only-PR” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Puerto Rico.
Recall timeline
FDA terminated this recall 6 months after the firm started it.
1Firm started the recall
2FDA classified it Class III
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-0484-2021 (April 20, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0484-2021 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 10, 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.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.