Katy's KITCHEN Originals LEMON GELATIN MIX MEXCLA DE GELATINA DE LIMON, NET WT. 24 OZ. (1.5 LBS.) 680 g, UPC 8 22486 117
Summary
The FDA issued a Class II for Katy's KITCHEN Originals LEMON GELATIN MIX MEXCLA DE GELATINA DE LIMON, NET WT. by DYMA BRANDS. Reason: 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.
Details
Source
Food Recall
External ID
F-0227-2025
Action Date
2024-12-11
Status
Ongoing
Category
food
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
Lot/Code Info: 50404: Lot 257 EZA
Quantity Affected: 27cs/12/24oz pouches (4 of each flavor)
Reason for Recall
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
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.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-10-02
Company
Atlanta, GA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 107 food recalls issued in the same week, part of 204 food-related FDA actions this month.
DYMA BRANDS has 21 FDA actions in our database, including 21 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (DYMA BRANDS) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does DYMA BRANDS have FDA actions?
DYMA BRANDS has 21 FDA actions in our database, including 21 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0227-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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