Class IIITerminated in FDA datasetRecall initiated Aug 21, 2024

MySyrup Sugar Free Peppermint Syrup. Product is packaged in the same square 0.5gallon HDPE…

Recalling firm: My Chai Inc

Why it was recalled

Acidified product is recalled due to lack production record.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Feb 3, 2026.

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ProductMySyrup Sugar Free Peppermint Syrup. Product is packaged in the same square 0.5gallon HDPE plastic bottles and the volume is 68 fl oz. Ingredients: Water, natural flavor, 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.
Package size68 fl oz

FDA code information

Batch numbers and Expiration Dates: RC011221-SFPPT 1/12/23 RC123021-SFPPT 12/30/23 AH042722-SFPPT 4/26/24 RC112322-SFPPT 11/22/24 RC120423-SFPPT 12/3/25

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Full FDA record and distribution details

Original product description

MySyrup Sugar Free Peppermint Syrup. Product is packaged in the same square 0.5gallon HDPE plastic bottles and the volume is 68 fl oz. Ingredients: Water, natural flavor, 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.

Original FDA recall reason

Acidified product is recalled due to lack production record.

Recall details

Recall number
F-0116-2025
Event ID
95346
FDA status
Terminated
Initiated
Aug 21, 2024
Reported
Nov 13, 2024
Classified
Nov 4, 2024
Terminated
Feb 3, 2026
Quantity
142 jugs
Location
Bend, OR, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

Nationwide

FDA source record · F-0116-2025

Data updated September 16, 2026. View official FDA data ↗

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