Fruit Punch Beverage Mix (DYMA Brands) – Metal Fragment Risk (2024)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Gordon CHOICE Fruit Punch Beverage Mix Naturally and Artificially Flavored Low Calorie Instant, NET WT. 8.6 OZ (243 g), UPC 0 93901 59606 2, Case UPC 10093901596069 & NET WT. 22OZ (1 LB 6 OZ) 624 g, 0 93901 28673 4, Case UPC 10093901286731, FOR DISTRIBUTION EXCLUSIVELY BY PARA SU DISTRIBUCION EXCLUSIVA POR GORDON FOOD SERVICE WYOMING, MI 49509
Brand
DYMA BRANDS
Lot Codes / Batch Numbers
50770: 8.6 oz - Lot #263 EGA & 50524: 22 oz - Lot 268 EFA
Products Sold
50770: 8.6 oz - Lot #263 EGA & 50524: 22 oz - Lot 268 EFA
DYMA BRANDS is recalling Gordon CHOICE Fruit Punch Beverage Mix Naturally and Artificially Flavored Low Calorie Instant, NET due to After an investigation, the firm discovered that a sifter used in the production of the Dextrose for each product was damaged and introduced metal fra. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AZ, AR, CA, CO, CT, FL, GA, IL, IA, LA, MD, MI, MN, MO, NE, NV, NJ, NM, NC, ND, OH, OK, OR, PA, TN, TX, UT, WA, WV, WI
Page updated: Jan 7, 2026