FDA recall record

DYMA BRANDS Katy's KITCHEN Originals LEMON GELATIN MIX MEXCLA DE GELATINA recall — FDA F-0227-2025

After an investigation, the firm discovered that a sifter used in the production of the Dextrose for each product was damaged and introduced metal…

Class IIclassification
F-0227-2025official record ID
Dec 11, 2024report date

Recall record at a glance

Official recordF-0227-2025
CategoryFood Recalls
ClassificationClass II
FDA record statusCompleted
Recalling firmDYMA BRANDS
Report dateDec 11, 2024
Recall initiation dateOct 2, 2024
Quantity27cs/12/24oz pouches (4 of each flavor)
LocationAtlanta, GA, United States

Official product description

Katy's KITCHEN Originals LEMON GELATIN MIX MEXCLA DE GELATINA DE LIMON, NET WT. 24 OZ. (1.5 LBS.) 680 g, UPC 8 22486 11794 8, Case UPC 30822486117918; Katy's KITCHEN Originals LIME GELATIN MIX, NET WT. 24 OZ. (1.5 LBS.) 680 g, UPC 8 22486 11795 5 & Katy's KITCHEN Originals ORANGE GELATIN MIX MEZCLA DE GELATINA DE NARANJA, NET WT. 24 OZ (1.5 LBS.) 680g, UPC 8 22486 11796 2, MARKETED BY INDEPENDENT MARKETING ALLIANCE HOUSTON, TX 77043

Why the product was recalled

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.

Distribution information

Products were distributed to the following states: AR, AZ, CA, CO, CT, FL, GA, IA, IL, LA, MD, MI, MN, MO, NC, ND, NE, NJ, NM, NV, OH, OK, OR, PA, TN, TX, UT, WA, WI & WV.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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