CLASS II Food recall · Reported 25 Sep 2013 · FDA Enforcement Report

Artichoke Pecorino Sauce/case recalled by Premier Foods

Premier Foods is recalling Artichoke Pecorino Sauce/case, distributed in Mississippi, New Jersey. The recall was initiated on 28 Aug 2013 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot#: 01813-16PF1, 01813-16PF2, 01813-16PF3, 01813-16PF4
Quantity recalled5880 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-1891-2013
FDA event ID
66142
Recalling firm
Premier Foods, Santa Fe Springs, CA
Classification
Class II
Status
Terminated
Recall initiated
28 Aug 2013
FDA classified
17 Sep 2013
Reported
25 Sep 2013
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Undeclared Soy
Product category
Sauces & Condiments

Timeline

28 Aug 2013Recall initiated by company
17 Sep 2013Classified by FDA+20 days
25 Sep 2013Published 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

Premier Foods is recalling Williams-Sonoma flavored sauces due to undeclared soy allergens (hydrolyzed soy protein).

Product as listed by the FDA

Artichoke Pecorino Sauce, 16 fl. oz., 12 jars/case

Where it was distributed

MS and NJ

MississippiNew Jersey

Questions about this recall

Why was it recalled?

Premier Foods is recalling Williams-Sonoma flavored sauces due to undeclared soy allergens (hydrolyzed soy protein).

Which lots are affected?

Lot#: 01813-16PF1, 01813-16PF2, 01813-16PF3, 01813-16PF4

Where was it sold?

MS and NJ

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.

Other products in this recall event

3 other products · FDA event 66142

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