RecallHawk
Class I Recall

Choi Heong Yuen Bakery Almond Cakes in round metal container Ingredients: mung bean powder (cereal containing gluten), s

fayeon distributors inc.

Summary

The FDA issued a Class I for Choi Heong Yuen Bakery Almond Cakes in round metal container Ingredients: mung b by fayeon distributors inc.. Reason: Product may contain undeclared milk.

Details

Source

Food Recall

External ID

F-0182-2023

Action Date

2022-12-07

Status

Terminated

Category

food

Product Description

Choi Heong Yuen Bakery Almond Cakes in round metal container Ingredients: mung bean powder (cereal containing gluten), sugar, almond (tree nuts), vegetable oil (canola oil), peanuts; (may contain traces of walnut, egg, and milk). Packed in cases of 12 units Store in cool, dry place 400g (14 oz.) UPC Code: 6 50495 00056 8 Made in Macau

Lot/Code Info: Lot Code 2239550054 Item number: CHY000568 Expiration date: 01/31/2024

Quantity Affected: 194 cases. 12 units per case

Reason for Recall

Product may contain undeclared milk

Distribution

A total of 20 customers received this product located in NY and CA

Type: Voluntary: Firm initiated

Recall Initiated: 2022-10-21

Company

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 16 food recalls issued in the same week, part of 204 food-related FDA actions this month.

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 (fayeon distributors inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does fayeon distributors inc. have FDA actions?

This is the only FDA action we have on record for fayeon distributors inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0182-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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