My Chai Inc Recall: Acidified product is recalled due to lack production record.

🇺🇸 United States

1. August 21, 2024 - Recall initiated
2. November 13, 2024 - Reported by source
3. February 3, 2026 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0117-2025

Event ID

95346

Status

Terminated

Classification

Class III

Company

My Chai Inc

Product description

MySyrup Sugar Free Raspberry Syrup. Product is packaged in the same square 0.5gallon HDPE plastic bottles and the volume is 68 fl oz. Ingredients: Water, natural flavor, vanilla extract, sodium benzoate and potassium sorbate (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.

Quantity

491 jugs

Reason

Acidified product is recalled due to lack production record.

Recall initiation date

August 21, 2024

Report date

November 13, 2024

Classification date

Not published in this source record

Termination date

February 3, 2026

Distribution pattern

Nationwide

UPC, lot, and code information

Batch numbers and Expiration Dates: RC010921-SFRAS 1/8/23 RC080221-SFRAS 8/2/23 RC121622-SFRAS 12/15/24 RC041823-SFRAS 4/17/25

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Telephone

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 95346 with 9 other product entries in Public Health Trace.

Responsible company: My Chai Inc

Other recalls from My Chai Inc

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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