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Mondelez Global Llc Recall: Undeclared FD&C Yellow No. 5

United States

TerminatedClass II

Company
Mondelez Global Llc
Product
Sour Patch Kids Watermelon Jelly Beans Net Wt.3 OZ (368g) UP…
Recall date
January 18, 2023
Terminated
September 28, 2023
Source
FDA

Reason for recall

Undeclared FD&C Yellow No. 5

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Sour Patch Kids Watermelon Jelly Beans Net Wt.3 OZ (368g) UPC: 0 70462 00719 0 24 bags per case Not published in this source record 14,611 cases Best buy dates 23JUN2023 through 13JUL2023

Distribution

  • Distributed to 81 consignees (retailers
  • wholesalers
  • military) nationwide

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0348-2023
Event ID
91537
Status
Terminated
Classification
Class II
Company
Mondelez Global Llc
Product description
Sour Patch Kids Watermelon Jelly Beans Net Wt.3 OZ (368g) UPC: 0 70462 00719 0 24 bags per case
Quantity
14,611 cases
Reason
Undeclared FD&C Yellow No. 5
Recall initiation date
January 18, 2023
Report date
February 15, 2023
Classification date
Not published in this source record
Termination date
September 28, 2023
Distribution pattern
Distributed to 81 consignees (retailers, wholesalers, military) nationwide
UPC, lot, and code information
Best buy dates 23JUN2023 through 13JUL2023
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Mondelez Global Llc

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Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.