Enjoy Premium Taro Cookies packaged in 5.3 oz. foil pouches and 17.7 oz clear bags
Summary
The FDA issued a Class I for Enjoy Premium Taro Cookies packaged in 5.3 oz. foil pouches and 17.7 oz clear ba by KTM Services, Inc.. Reason: Undeclared allergens; milk.
Details
Source
Food Recall
External ID
F-0035-2025
Action Date
2024-10-23
Status
Terminated
Category
food
Product Description
Enjoy Premium Taro Cookies packaged in 5.3 oz. foil pouches and 17.7 oz clear bags
Lot/Code Info: Best By Dates: 09/12/2024 - 08/07/2025
Quantity Affected: 5.3 oz. Taro Cookies: 17,288 units; 17.7 oz. Taro Cookies: 2,241 units
Reason for Recall
Undeclared allergens; milk
Distribution
Products were sold in Hawaii, Guam, and Nevada retail stores and via web sales.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-09-13
Company
Honolulu, HI
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 33 food recalls issued in the same week, part of 204 food-related FDA actions this month.
KTM Services, Inc. has 2 FDA actions in our database, including 2 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 (KTM Services, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does KTM Services, Inc. have FDA actions?
KTM Services, Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0035-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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