Fruit flavored ready-to-eat cereal packaged in 1.27 oz. (UPC 850017468214) and 8oz. ( UPC 850017468085) plastic stand up
Summary
The FDA issued a Class II for Fruit flavored ready-to-eat cereal packaged in 1.27 oz. (UPC 850017468214) and 8 by Catalina Snacks. Reason: Foreign material - metal..
Details
Source
Food Recall
External ID
F-0612-2023
Action Date
2023-03-22
Status
Terminated
Category
food
Product Description
Fruit flavored ready-to-eat cereal packaged in 1.27 oz. (UPC 850017468214) and 8oz. ( UPC 850017468085) plastic stand up pouch.
Lot/Code Info: Best By Date 8/1/2023
Quantity Affected: 316,980 pouches.
Reason for Recall
Foreign material - metal.
Distribution
NY, CA, CO, IA, KY, TX, AZ, GA, FL, MD, IN, PA, IL, OR, NJ, OK, VA, NV, NH, WI, CT, Online sales
Type: Voluntary: Firm initiated
Recall Initiated: 2023-02-15
Company
Lebanon, IN
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 488 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Catalina Snacks has 7 FDA actions in our database, including 7 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 (Catalina Snacks) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Catalina Snacks have FDA actions?
Catalina Snacks has 7 FDA actions in our database, including 7 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0612-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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