Pamana Brand Mini Fruit Jelly Cup 35.27 oz. Lychee Flavor 6 units per case Item #416704
Summary
The FDA issued a Class I for Pamana Brand Mini Fruit Jelly Cup 35.27 oz. Lychee Flavor 6 units per case Item by Foremost Foods International, Inc.. Reason: Potential choking hazard.
Details
Source
Food Recall
External ID
F-1303-2023
Action Date
2023-08-09
Status
Terminated
Category
food
Product Description
Pamana Brand Mini Fruit Jelly Cup 35.27 oz. Lychee Flavor 6 units per case Item #416704
Lot/Code Info: UPC 795981293021
Quantity Affected: 11,040 units (total of all 3 products)
Reason for Recall
Potential choking hazard
Distribution
Throught the United States and one distributor in Mississauga, ON, Canada
Type: Voluntary: Firm initiated
Recall Initiated: 2023-06-12
Company
Pomona, CA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 71 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Foremost Foods International, Inc. has 6 FDA actions in our database, including 6 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Foremost Foods International, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Foremost Foods International, Inc. have FDA actions?
Foremost Foods International, Inc. has 6 FDA actions in our database, including 6 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1303-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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