BTREX PLUS Dietary Supplement Recalled for Damaged Tablets
Lopez Gonzalez Santana Corporation is recalling BTREX PLUS dietary supplements due to damaged tablets, a cGMP deviation.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The recall is classified as FDA Class III, which indicates the product is not likely to cause adverse health consequences. The issue is a cosmetic defect (damaged tablets) with no reported injuries.
Plain-English summary
Lopez Gonzalez Santana Corporation is voluntarily recalling 311 bottles of BTREX PLUS, Dietary Supplement 100 Caplets. The recall is due to a Current Good Manufacturing Practice (cGMP) deviation involving the presence of damaged tablets.
The affected product is identified by Lot # 33277 and has an expiration date of 12/22. The product was distributed domestically in Puerto Rico.
Consumers with this product should stop using it and contact the recalling firm for further instructions.
The recalled product
- Product
- BTREX PLUS, Dietary Supplement 100 Caplets
- Manufacturer
- Lopez Gonzalez Santana Corporation
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 311
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot # 33277 Exp date:12/22
Distribution
Distribution scope not specified by the agency.
Related recalls
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