CLASS II Food recall · Reported 1 Apr 2015 · FDA Enforcement Report

Buffalo Wing Sauce recalled by Stonewall Kitchen

Stonewall Kitchen is recalling Buffalo Wing Sauce, distributed in 24 states. The recall was initiated on 3 Mar 2015 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesEnjoy By Date: 06Feb2017

Quantity recalled327 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-1619-2015
FDA event ID: 70640
Recalling firm: Stonewall Kitchen, York, ME
Brand: Buffalo Wing
Classification: Class II
Status: Terminated
Recall initiated: 3 Mar 2015
FDA classified: 26 Mar 2015
Reported: 1 Apr 2015
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Undeclared Soy
Product category: Sauces & Condiments

Timeline

3 Mar 2015	Recall initiated by company
26 Mar 2015	Classified by FDA	+23 days
1 Apr 2015	Published in enforcement report	+6 days

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

Reason for recall

Undeclared soy lecithin

Product as listed by the FDA

Stonewall Kitchen Buffalo Wing Sauce Net Wt. 17.5 oz. glass jar UPC 711381-31395 4 Item # 251805,

Where it was distributed

AK, AZ, CA, CT, FL, IA, IL, MA, MD, ME, MI, MO, MS, MT, ND, NH, NJ, NY, OH, SC, UT, VA, VT, WI

Alaska Arizona California Connecticut Florida Iowa Illinois Massachusetts Maryland Maine Michigan Missouri Mississippi Montana North Dakota New Hampshire New Jersey New York Ohio South Carolina

Questions about this recall

Why was it recalled?

Undeclared soy lecithin

Which lots are affected?

Enjoy By Date: 06Feb2017

Where was it sold?

AK, AZ, CA, CT, FL, IA, IL, MA, MD, ME, MI, MO, MS, MT, ND, NH, NJ, NY, OH, SC, UT, VA, VT, WI

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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