CLASS II Food recall · Reported 27 Nov 2013 · FDA Enforcement Report

Idahoan, Steakhouse Parmesan topping recalled by Kerry Foods

Kerry Foods is recalling Idahoan, Steakhouse Parmesan topping, distributed in Idaho. The recall was initiated on 13 Sep 2013 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot 3239

Quantity recalled10,500 lbs. (300 x 35 pound units)

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-0181-2014
FDA event ID: 66329
Recalling firm: Kerry Foods, Beloit, WI
Brand: Idahoan
Classification: Class II
Status: Terminated
Recall initiated: 13 Sep 2013
FDA classified: 18 Nov 2013
Reported: 27 Nov 2013
Type: Voluntary: Firm initiated
Customers notified by: Telephone
Reason category: Salmonella
Product category: Cheese

Timeline

13 Sep 2013	Recall initiated by company
18 Nov 2013	Classified by FDA	+66 days
27 Nov 2013	Published 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

Steakhouse Parmmesan Topping was produced on the same equipment line as another product that tested positive for 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

Idahoan, Steakhouse Parmesan topping, Net Weight 35 lbs., Item Code ZID800Bulk.

Where it was distributed

Idaho

Questions about this recall

Why was it recalled?

Steakhouse Parmmesan Topping was produced on the same equipment line as another product that tested positive for Salmonella.

Which lots are affected?

Lot 3239

Where was it sold?

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 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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