CLASS II Food recall · Reported 10 May 2017 · FDA Enforcement Report

Chili Spice Blend in packets recalled by Arro

Arro is recalling Chili Spice Blend in packets, distributed in Ohio. The recall was initiated on 29 Mar 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLots: 5389705300AA, 5389705400AA
Quantity recalled67,500 pouches (150 cases).

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-2141-2017
FDA event ID
76903
Recalling firm
Arro, Hodgkins, IL
Brand
Chili
Classification
Class II
Status
Terminated
Recall initiated
29 Mar 2017
FDA classified
28 Apr 2017
Reported
10 May 2017
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Salmonella
Product category
Spices

Timeline

29 Mar 2017Recall initiated by company
28 Apr 2017Classified by FDA+30 days
10 May 2017Published in enforcement report+12 days

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

Reason for recall

Possible contamination of chili seasoning mix with Salmonella.

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

10.0 Grams Chili Spice Blend in packets

Where it was distributed

OH

Ohio

Questions about this recall

Is Chili Spice Blend in packets recalled?

Yes. Arro recalled Chili Spice Blend in packets on 29 Mar 2017. The recall is Class II and its status is Terminated. Recall number F-2141-2017.

Why was it recalled?

Possible contamination of chili seasoning mix with Salmonella.

Which lots are affected?

Lots: 5389705300AA, 5389705400AA

Where was it sold?

OH

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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