Wegmans Potato Salad Recall: Undeclared Egg in Family Pack
Wegmans recalls 48oz potato salad due to undeclared egg in ingredients. This affects consumers with egg allergies. No remedy specified in official notice.
Lower-risk recall
Wegman's Potato Salad, Net Wt. 48 oz is being recalled for undeclared egg as the containers were labeled with a nutritional and ingredient statement from a different product.
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What happened, in plain English
Wegmans is recalling a 48-ounce family pack potato salad because it contains undeclared egg. This poses a risk for people with egg allergies who may react to the egg in the product. Read more at govinfonow.com/recall/21411-wegmans-potato-salad-recall-undeclared-egg-in-family-pack.
Source Summary by GovInfoNow · govinfonow.com/recall/21411-wegmans-potato-salad-recall-undeclared-egg-in-family-pack · Updated October 8, 2026 · FDA enforcement record: FDA #F-2240-2017
Cite this page
“Wegmans Potato Salad Recall: Undeclared Egg in Family Pack.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21411-wegmans-potato-salad-recall-undeclared-egg-in-family-pack. Based on FDA recall #F-2240-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2240-2017%22&limit=1).
Why it’s dangerous
The product was labeled with a nutritional statement from a different product, so egg was not declared as an ingredient. This means individuals with egg allergies could consume the product without knowing, leading to potential allergic reactions.
Who’s affected
People with egg allergies are at risk from this potato salad. The recall affects consumers who purchased the Wegmans Family Pack Potato Salad.
How to tell if you have this one
Check for Wegmans Family Pack Potato Salad with a 48-ounce net weight. The product contains pasta shells, water, cucumbers, and feta cheese. It was distributed by Wegmans Food Markets in Rochester, NY.
- Brand
Wegmans- Product
Wegmans Wegmans Family Pack Potato Salad, Net Wt. 48 OZ; Ingredients: Pasta Shells***Water, Cucumbers, Feta- Category
Food
What to do — step by step
Check Product Label
Look for the product name and net weight of 48 ounces on the label.
Where it went and when
Where it was distributed
Distributed in 3 states.
FDA distribution: “MA, NY, PA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Massachusetts, New York, Pennsylvania.
Recall timeline
FDA terminated this recall 7 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-2240-2017 (May 5, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2240-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 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.