Frios Gourmet Pops - Creamy Coconut Popsicle 3oz frozen popsicle packaged individually in clear plastic sleeve. 48 popsi
Summary
The FDA issued a Class II for Frios Gourmet Pops - Creamy Coconut Popsicle 3oz frozen popsicle packaged indivi by FGP Manufacturing, LLC. Reason: Undeclared sulfites.
Details
Source
Food Recall
External ID
F-1036-2024
Action Date
2024-03-13
Status
Terminated
Category
food
Product Description
Frios Gourmet Pops - Creamy Coconut Popsicle 3oz frozen popsicle packaged individually in clear plastic sleeve. 48 popsicles per box. *Sold directly to end consumer via food truck
Lot/Code Info: Manufacturer No. 010212
Quantity Affected: 329 boxes (48/bx)
Reason for Recall
Undeclared sulfites
Distribution
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.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-02-07
Company
Mobile, AL
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 124 food recalls issued in the same week, part of 204 food-related FDA actions this month.
FGP Manufacturing, LLC has 3 FDA actions in our database, including 3 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 (FGP Manufacturing, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does FGP Manufacturing, LLC have FDA actions?
FGP Manufacturing, LLC has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1036-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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