CLASS I Food recall · Reported 18 Oct 2017 · FDA Enforcement Report

waterfront Bistro Tatar Sauce recalled by Silver Spring Foods

Silver Spring Foods is recalling waterfront Bistro Tatar Sauce, distributed nationwide in the US. The recall was initiated on 22 Sep 2017 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBest By date of JUL 31 18 S3351 and AUG 28 18 S3351
Quantity recalled11092 cases (6 bottles per case)

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-0019-2018
FDA event ID
78176
Recalling firm
Silver Spring Foods, Eau Claire, WI
Classification
Class I
Status
Terminated
Recall initiated
22 Sep 2017
FDA classified
10 Oct 2017
Reported
18 Oct 2017
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Other Reasons
Product category
Sauces & Condiments

Timeline

22 Sep 2017Recall initiated by company
10 Oct 2017Classified by FDA+18 days
18 Oct 2017Published 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

Silver Spring is recalling Waterfront Bistro Tartar Sauce because an incorrect back label does not identify egg.

Product as listed by the FDA

waterfront Bistro Tatar Sauce, Net Wt 9 oz. (255g), UPC 21130-12242

Where it was distributed

Nationwide: AR, AZ, CA, DE, FL, HI, IA, ID,IL, IN, LA, MA, MD, ME, MT, ND, NE, NH, NM, NV, OR, RI, SD, TX, UT, VT, VA, WA, WY, including Washington DC

Nationwide ArkansasArizonaCaliforniaDistrict of ColumbiaDelawareFloridaHawaiiIowaIdahoIllinoisIndianaLouisianaMassachusettsMarylandMaineMontanaNorth DakotaNebraskaNew HampshireNew Mexico

Questions about this recall

Why was it recalled?

Silver Spring is recalling Waterfront Bistro Tartar Sauce because an incorrect back label does not identify egg.

Which lots are affected?

Best By date of JUL 31 18 S3351 and AUG 28 18 S3351

Where was it sold?

Nationwide: AR, AZ, CA, DE, FL, HI, IA, ID,IL, IN, LA, MA, MD, ME, MT, ND, NE, NH, NM, NV, OR, RI, SD, TX, UT, VT, VA, WA, WY, including Washington DC

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 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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