Sour Patch Kids Watermelon Jelly Beans Net Wt.3 OZ (368g) UPC: 0 70462 00719 0 24 bags per case
Summary
The FDA issued a Class II for Sour Patch Kids Watermelon Jelly Beans Net Wt.3 OZ (368g) UPC: 0 70462 00719 0 2 by Mondelez Global Llc. Reason: Undeclared FD&C Yellow No. 5.
Details
Source
Food Recall
External ID
F-0348-2023
Action Date
2023-02-15
Status
Terminated
Category
food
Product Description
Sour Patch Kids Watermelon Jelly Beans Net Wt.3 OZ (368g) UPC: 0 70462 00719 0 24 bags per case
Lot/Code Info: Best buy dates 23JUN2023 through 13JUL2023
Quantity Affected: 14,611 cases
Reason for Recall
Undeclared FD&C Yellow No. 5
Distribution
Distributed to 81 consignees (retailers, wholesalers, military) nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2023-01-18
Company
East Hanover, NJ
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 30 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Mondelez Global Llc has 13 FDA actions in our database, including 13 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 (Mondelez Global Llc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Mondelez Global Llc have FDA actions?
Mondelez Global Llc has 13 FDA actions in our database, including 13 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0348-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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