CLASS II Food recall · Reported 27 Sep 2017 · FDA Enforcement Report

El Chilar Whole Ginger recalled

EL Chilar Huff is recalling El Chilar Whole Ginger. The recall was initiated on 4 Aug 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Number 918 (expiration date: 09/2018)
Quantity recalled1236 units (103 dozens)

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-3572-2017
FDA event ID
77931
Recalling firm
EL Chilar Huff, Apopka, FL
Classification
Class II
Status
Terminated
Recall initiated
4 Aug 2017
FDA classified
20 Sep 2017
Reported
27 Sep 2017
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Sulfites
Product category
Other

Timeline

4 Aug 2017Recall initiated by company
20 Sep 2017Classified by FDA+47 days
27 Sep 2017Published in enforcement report+7 days

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

Reason for recall

Product contains undeclared sulfites.

Product as listed by the FDA

El Chilar Whole Ginger, NET WT 1.25 Oz (35g)

Where it was distributed

U.S. Consignees only.

Questions about this recall

Is El Chilar Whole Ginger recalled?

Yes. EL Chilar Huff recalled El Chilar Whole Ginger on 4 Aug 2017. The recall is Class II and its status is Terminated. Recall number F-3572-2017.

Why was it recalled?

Product contains undeclared sulfites.

Which lots are affected?

Lot Number 918 (expiration date: 09/2018)

Where was it sold?

U.S. Consignees only.

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 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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