CLASS I Food recall · Reported 2 Apr 2014 · FDA Enforcement Report

L-Citrulline, bulk product recalled by Axel Chemicals

Axel Chemicals is recalling L-Citrulline, bulk product, distributed in North Carolina, New Jersey, New York. The recall was initiated on 24 Feb 2014 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot number 121109
Quantity recalled1000 kg

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1685-2014
FDA event ID
67616
Recalling firm
Axel Chemicals, Brentwood, TN
Classification
Class I
Status
Terminated
Recall initiated
24 Feb 2014
FDA classified
25 Mar 2014
Reported
2 Apr 2014
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Other Reasons
Product category
Other

Timeline

24 Feb 2014Recall initiated by company
25 Mar 2014Classified by FDA+29 days
2 Apr 2014Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

The recall was initiated due to an adverse event report from a consignee and the discovery of a compound other than L-Citrulline in at least one drum.

Product as listed by the FDA

L-Citrulline, bulk product, 25 kg

Where it was distributed

NY, NJ, and NC

North CarolinaNew JerseyNew York

Questions about this recall

Why was it recalled?

The recall was initiated due to an adverse event report from a consignee and the discovery of a compound other than L-Citrulline in at least one drum.

Which lots are affected?

Lot number 121109

Where was it sold?

NY, NJ, and NC

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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