Class IITerminated in FDA datasetRecall initiated Jan 15, 2018

Jarrow Formulas Liquid L-Carnitine; 16 fl oz. (475 ml) bottle, dietary supplement; product…

Recalling firm: Jarrow Formulas Inc

Why it was recalled

A higher than normal micro result was found at the six month time point for one lot of Liquid L-Carnitine.

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: Jul 10, 2018.

Check your package

Compare the exact product and package details with the label you have.

ProductJarrow Formulas Liquid L-Carnitine; 16 fl oz. (475 ml) bottle, dietary supplement; product number 102006; UPC 7 90011 02006 6; Vitamin B5 10 mg; L-Carnitine 1000 mg; Other ingredients: Purified water, xylitol, glycerin, citric acid, natural lemon-lime flavor, nisin (as a preservative). Distributed exclusively by Jarrow Formulas Los Angeles, CA.
Package size16 fl oz
UPC790011020066

FDA code information

Lot Number: JLC17131; Expiration date: 05/2019

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Jarrow Formulas Liquid L-Carnitine; 16 fl oz. (475 ml) bottle, dietary supplement; product number 102006; UPC 7 90011 02006 6; Vitamin B5 10 mg; L-Carnitine 1000 mg; Other ingredients: Purified water, xylitol, glycerin, citric acid, natural lemon-lime flavor, nisin (as a preservative). Distributed exclusively by Jarrow Formulas Los Angeles, CA.

Extracted codes and context

TypeCode / valueContext
UPC790011020066ne; 16 fl oz. (475 ml) bottle, dietary supplement; product number 102006; UPC 7 90011 02006 6; Vitamin B5 10 mg; L-Carnitine 1000 mg; Other ingredients: Purified water, xylitol, glycerin, citric acid, natural
lotJLC17131Lot Number: JLC17131; Expiration date: 05/2019

Original FDA recall reason

A higher than normal micro result was found at the six month time point for one lot of Liquid L-Carnitine.

Recall details

Recall number
F-0682-2018
Event ID
78967
FDA status
Terminated
Initiated
Jan 15, 2018
Reported
Feb 7, 2018
Classified
Jan 30, 2018
Terminated
Jul 10, 2018
Quantity
2853 units
Location
Los Angeles, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Nationwide distribution

FDA source record · F-0682-2018

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

Follow official FDA and manufacturer guidance.