Silver Spring Waterfront Bistro Tatar Sauce Recall: Egg Not Listed on Label
Silver Spring Foods recalls 9oz Waterfront Bistro Tatar Sauce due to missing egg ingredient on label. Consumers should check UPC 21130-12242 and best by dates.
Lower-risk recall
Silver Spring is recalling Waterfront Bistro Tartar Sauce because an incorrect back label does not identify egg.
Contact the company
What happened, in plain English
Silver Spring Foods is recalling their Waterfront Bistro Tatar Sauce because the product label does not list eggs as an ingredient. This could be a problem for people with egg allergies who might consume the sauce without knowing. Read more at govinfonow.com/recall/20406-silver-spring-waterfront-bistro-tatar-sauce-recall-egg-not-listed.
Source Summary by GovInfoNow · govinfonow.com/recall/20406-silver-spring-waterfront-bistro-tatar-sauce-recall-egg-not-listed · Updated October 7, 2026 · FDA enforcement record: FDA #F-0019-2018
Cite this page
“Silver Spring Waterfront Bistro Tatar Sauce Recall: Egg Not Listed on Label.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20406-silver-spring-waterfront-bistro-tatar-sauce-recall-egg-not-listed. Based on FDA recall #F-0019-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0019-2018%22&limit=1).
Why it’s dangerous
The sauce label does not identify eggs as an ingredient. This means consumers with egg allergies might unknowingly eat the sauce and experience an allergic reaction.
Who’s affected
People who purchased Waterfront Bistro Tatar Sauce with UPC 21130-12242 from stores that sold it before August 2018 are likely affected. Those with egg allergies are at higher risk.
How to tell if you have this one
Check for the UPC 21130-12242 on the sauce container. The product was sold with best by dates of July 31, 2018 or August 28, 2018.
- Brand
Silver Spring- Product
waterfront Bistro Tatar Sauce, Net Wt 9 oz. (255g), UPC 21130-12242- Category
Food
What to do — step by step
Check Label
Look for the UPC 21130-12242 on the sauce container to confirm it's the recalled product.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 29 states.
FDA distribution: “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” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Arizona, Arkansas, California, Delaware, District of Columbia, Florida, Hawaii, Idaho, Illinois, Indiana, Iowa, Louisiana, Maine, Maryland, Massachusetts, Montana, Nebraska, Nevada, New Hampshire, New Mexico, North Dakota, Oregon, Rhode Island, South Dakota, Texas, Utah, Vermont, Virginia, Washington, Wyoming.
Recall timeline
FDA terminated this recall 21 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-0019-2018 (September 22, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0019-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.