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Lower risk Food recall · FDA · Published January 15, 2018

Jarrow Formulas Liquid L-Carnitine Recall: Higher Micro Result at 6 Months

Jarrow Formulas recalls 16 fl oz L-Carnitine supplements with a higher than normal micro result at six months. This dietary supplement may pose a risk for some users. Check product details to see if you have the affected batch.

🇺🇸 FDA recall #F-0682-2018FoodJarrow Formulas ›
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Recalling firmJarrow Formulas Inc1824 S Robertson Blvd · Los Angeles, CA 90035-4317
✎ GovInfoNow plain-language explainer

What happened, in plain English

Jarrow Formulas is recalling a specific liquid L-Carnitine supplement due to a higher than normal micro result found in one lot at the six-month time point. This issue could affect users who consumed the product over time, though the exact risk is not specified in the recall. Read more at govinfonow.com/recall/19800-jarrow-formulas-liquid-l-carnitine-recall-higher-micro-result-at.

Source Summary by GovInfoNow · govinfonow.com/recall/19800-jarrow-formulas-liquid-l-carnitine-recall-higher-micro-result-at · Updated October 7, 2026 · FDA enforcement record: FDA #F-0682-2018

Cite this page

“Jarrow Formulas Liquid L-Carnitine Recall: Higher Micro Result at 6 Months.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19800-jarrow-formulas-liquid-l-carnitine-recall-higher-micro-result-at. Based on FDA recall #F-0682-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0682-2018%22&limit=1).

Why it’s dangerous

The recall is based on a higher than normal micro result detected in one specific lot of the product at the six-month time point. This suggests a potential issue with the product's stability or quality over time, but the exact mechanism is not detailed in the recall.

Who’s affected

People who purchased the Jarrow Formulas Liquid L-Carnitine 16 fl oz bottle with product number 102006 or UPC 7 90011 are affected. Those who have been using the product for six months or longer may be at slightly higher risk.

How to tell if you have this one

Check for the product number 102006 or UPC 7 90011 on the bottle. The affected product is a 16 fl oz (475 ml) liquid L-Carnitine dietary supplement with a lot number of JLC17131 and expiration date of May 2019.

  • Brand
    Jarrow Formulas
  • Product
    Jarrow Formulas Liquid L-Carnitine; 16 fl oz. (475 ml) bottle, dietary supplement; product number 102006; UPC 7 90011
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the product number 102006 or UPC 7 90011 on the bottle to confirm if it is affected.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide distribution” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 6 months after the firm started it.

1. Firm started the recall: Jan 15, 201812. FDA classified it Class II: Jan 30, 201823. Published in FDA’s Enforcement Report: Feb 7, 201834. FDA terminated the recall: Jul 10, 201842018
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-0682-2018 (January 15, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0682-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA