PreGel Lemon 50 recall
Recalled by PreGel America, Inc. · Concord, NC, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Undeclared Milk. The firm received a complaint that there was milk in the product. The product ingredient statement does not include milk.
Undeclared allergen: Milk
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
PreGel Lemon 50 4.4 lb (2kg) bag, Ingredients: dextrose, citric acid, mono and diglycerides of fatty acids, propane -1,2-diol esters of fatty acids, maltodextrins, carboxymethylcellulose, guar gum, flavors, dehydrated lemon juice, xanthan gum Manufactured by: PreGel America, Inc., 4450 Fortune Ave. NW Concord, NC 28027 USA Tel. +1 704-707-0300 UPC 0 817304 015148
Quantity: 179 cs/8/4.4 lb bags
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot 381081U279N Produced 04/18/2018 Best Before 04/17/2020, Product Code: 306038
Where it was sold
Arkansas California Colorado District of Columbia Florida Georgia Hawaii Iowa Illinois Indiana Kansas Massachusetts Minnesota Mississippi North Carolina New Jersey Nevada Oklahoma Oregon Pennsylvania South Carolina Tennessee Texas Utah Virginia Vermont Washington Wisconsin
FDA's distribution note: Product was shipped to the following states: AR, CA, CO, DC, FL, GA, HI, IA, IL, IN, KS, MA, MN, MS, NC, NJ, NV, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA & WI. Product was also shipped to Canada, Guatemala & St. Lucia.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to milk; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- PreGel America, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 2, 2019
- In FDA report of
- Sep 4, 2019
- Terminated
- Dec 17, 2021
- FDA recall number
- F-2108-2019 · event 83483
- Official record
- FDA enforcement report search