ICE CREAM BAR, MICHOACANA, es...natural, ROMPOPE, Net. Wt. 6 Fl. Oz., Packaged in a plastic bag. Frozen.
Summary
The FDA issued a Class II for ICE CREAM BAR, MICHOACANA, es...natural, ROMPOPE, Net. Wt. 6 Fl. Oz., Packaged i by La Michoacana 100% Natural Inc. Reason: Undeclared Yellow #5, Yellow #6, and Red #40.
Details
Source
Food Recall
External ID
F-0603-2024
Action Date
2023-12-27
Status
Terminated
Category
food
Product Description
ICE CREAM BAR, MICHOACANA, es...natural, ROMPOPE, Net. Wt. 6 Fl. Oz., Packaged in a plastic bag. Frozen.
Lot/Code Info: None
Quantity Affected: 170 units of 6 fl. oz. each
Reason for Recall
Undeclared Yellow #5, Yellow #6, and Red #40
Distribution
Domestic distribution only within the state of Florida.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-10-16
Company
Homestead, FL
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 157 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (La Michoacana 100% Natural Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does La Michoacana 100% Natural Inc have FDA actions?
This is the only FDA action we have on record for La Michoacana 100% Natural Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0603-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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