RecallHawk
Class III Recall

MySyrup Sugar Free Coconut Syrup. Product is packaged in the same square 0.5gallon HDPE plastic bottles and the volume i

My Chai Inc

Summary

The FDA issued a Class III for MySyrup Sugar Free Coconut Syrup. Product is packaged in the same square 0.5gall by My Chai Inc. Reason: Acidified product is recalled due to lack production record..

Details

Source

Food Recall

External ID

F-0113-2025

Action Date

2024-11-13

Status

Terminated

Category

food

Product Description

MySyrup Sugar Free Coconut Syrup. Product is packaged in the same square 0.5gallon HDPE plastic bottles and the volume is 68 fl oz. Ingredients: Water, natural flavor, potassium sorbate and sodium benzoate (to protect flavor), sucralose, acesulfame potassium, citric acid. Made by: MyChai, Inc. 1110 SE Centennial St. # 6, Bend, OR 97702. Up until fall of 2023, expiration dates were 2 years from the date of production. In the fall of 2023 expiration dates were extended an additional year to 3 years from the production date.

Lot/Code Info: Batch numbers and Expiration Dates: RC062521-SFCOC 6/25/23 RC032121-SFCOC 3/21/23 AH042622-SFCOC 4/25/24

Quantity Affected: 297 jugs

Reason for Recall

Acidified product is recalled due to lack production record.

Distribution

Nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2024-08-21

Company

My Chai Inc

Bend, OR

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 55 food recalls issued in the same week, part of 204 food-related FDA actions this month.

My Chai Inc has 14 FDA actions in our database, including 14 recalls.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 (My Chai Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does My Chai Inc have FDA actions?

My Chai Inc has 14 FDA actions in our database, including 14 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0113-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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