DYMA BRANDS recalls SYSCO VANILLA INSTANT (24oz case) due to metal fragments from damaged sifter in production. Consumers should check UPC 10074865103791 and lot 268 ECA 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 SYSCO VANILLA INSTANT (24oz case) because metal fragments were found in the product due to a damaged sifter during production. This poses a risk of injury if metal pieces are consumed.
During production, a damaged sifter introduced metal fragments into the vanilla instant product. If consumed, these metal pieces could cause injury, such as cuts or internal damage.
Consumers who purchased SYSCO VANILLA INSTANT (24oz case) with UPC 10074865103791 and lot 268 ECA from distributors in Houston, Texas are affected. People who consume the product may risk injury from metal fragments.
Check for the UPC 10074865103791 on the product case and lot number 268 ECA. The product was distributed by SYSCO CORPORATION in Houston, Texas.
Look for UPC 10074865103791 and lot number 268 ECA on the product case.
The recall is due to metal fragments introduced into the product during production because a sifter was damaged.
Check for UPC 10074865103791 and lot number 268 ECA on the product case.
The official notice 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-0239-2025 — DYMA BRANDS DYMA BRANDS Hello, I own a DYMA BRANDS that is covered by recall F-0239-2025 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.