CLASS I Food recall · Reported 8 Apr 2015 · FDA Enforcement Report

Cajun Seasoning recalled by The Spicemill

The Spicemill is recalling Cajun Seasoning, distributed in Connecticut. The recall was initiated on 28 Jan 2015 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot Code: 1432421, Best By: 12/16,1/17
Quantity recalled102 bottles

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-1796-2015
FDA event ID
70423
Recalling firm
The Spicemill, Manchester, CT
Brand
Cajun
Classification
Class I
Status
Terminated
Recall initiated
28 Jan 2015
FDA classified
30 Mar 2015
Reported
8 Apr 2015
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Peanuts
Product category
Spices

Timeline

28 Jan 2015Recall initiated by company
30 Mar 2015Classified by FDA+61 days
8 Apr 2015Published in enforcement report+9 days

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

Reason for recall

Product may contain undeclared peanut protein.

Product as listed by the FDA

Cajun Seasoning, 4 oz., UPC: 811267011735. Product is packaged in a plastic bottle with a black flip-top lid.

Where it was distributed

Product was distributed in the State of CT.

Connecticut

Questions about this recall

Is Cajun Seasoning recalled?

Yes. The Spicemill recalled Cajun Seasoning on 28 Jan 2015. The recall is Class I and its status is Terminated. Recall number F-1796-2015.

Why was it recalled?

Product may contain undeclared peanut protein.

Which lots are affected?

Lot Code: 1432421, Best By: 12/16,1/17

Where was it sold?

Product was distributed in the State of CT.

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 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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