Frios Gourmet Pops
Reason Undeclared sulfites
Frios Gourmet Pops recall
Recalled by FGP Manufacturing, LLC · Mobile, AL, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Undeclared Allergens - Egg
Undeclared allergen: Egg
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
Frios Gourmet Pops - Banana Pudding Popsicle 3oz frozen popsicle packaged individually in clear plastic sleeve. 48 popsicles per box. *Sold directly to end consumer via food truck
Quantity: 583 boxes (48/bx)
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.
Manufacturer No. 010212
Where it was sold
Alabama Arizona Colorado Florida Georgia Michigan Missouri North Carolina New Jersey Ohio Oklahoma Pennsylvania South Carolina Tennessee Texas Wisconsin West Virginia
FDA's distribution note: Distribution States: FL, OK, OH, SC, TX, CO, GA, WI, NC, AL, MO, WV, PA, MI, TN, AZ, NJ Product sent to franchise owners. -Banana Pudding pops manufactured between 2/21/23 - 1/17/24 and distributed between 2/26/23 - 2/6/24 to the customers on the list provided. -Creamy Coconut pops manufactured between 5/4/23 - 1/18/24 and distributed between 5/8/23 - 2/6/24 to the customers on the list provided. -Fruity Pebble pops manufactured between manufactured between 2/9/23 - 12/8/23 and distributed between 2/13/23 - 2/6/24 to the customers on the list provided.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to egg; 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
- FGP Manufacturing, LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 7, 2024
- In FDA report of
- Mar 13, 2024
- Terminated
- Apr 16, 2024
- FDA recall number
- F-1035-2024 · event 93970
- Official record
- FDA enforcement report search
Also recalled with it (2 more products)
FDA files each product of one recall action separately; these share the same FDA event.
Frios Gourmet Pops
Reason Undeclared Color Additives - Yellow #5