DYMA BRANDS recalls THIRSTER Low Cal Fruit (8.6oz) due to metal fragments from damaged sifter in production. Consumers should check UPC 50758108397380 and lot 263 EGA for affected items.
After an investigation, the firm discovered that a sifter used in the production of the Dextrose for each product was damaged and introduced metal fragments in the products.
DYMA BRANDS is recalling THIRSTER Low Cal Fruit products because metal fragments were found in the product during production. This could cause injury if consumed, so affected consumers should stop using the product and contact the manufacturer.
During production, a damaged sifter introduced metal fragments into the Dextrose used for the product. If these fragments are consumed, they could cause injury such as cuts or internal damage.
Consumers who purchased THIRSTER Low Cal Fruit (8.6oz) with UPC 50758108397380 and lot number 263 EGA are affected. Those who have consumed the product are at higher risk of injury from metal fragments.
Check for the product name 'THIRSTER Low Cal Fruit', net weight 8.6oz, and UPC 50758108397380. The lot number 263 EGA is also associated with this recall.
Look for the UPC 50758108397380 and lot number 263 EGA on the product label.
No, the product contains metal fragments that could cause injury if consumed.
Check for the UPC 50758108397380 and lot number 263 EGA on the product label.
The recall does not specify a remedy, so contact DYMA BRANDS for further instructions.
We’ve drafted a message you can send DYMA BRANDS to request your refund or repair — edit it as you like.
Subject: Recall F-0241-2025 — DYMA BRANDS DYMA BRANDS Hello, I own a DYMA BRANDS that is covered by recall F-0241-2025 from DYMA BRANDS. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.