“Wegmans Penne Salad Recall: Undeclared Milk Allergen Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/11089-wegmans-penne-salad-recall-undeclared-milk-allergen-risk. Based on FDA recall #F-0998-2023 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0998-2023%22&limit=1).
The FDA announced on May 25, 2023, that ASK Foods Inc is recalling Wegmans Penne Rigate Mozzarella Salad due to undeclared milk allergens. The voluntary recall affects 600 units distributed to stores in New York, Pennsylvania, and Massachusetts.
How to tell if you have it
Brand: Wegmans
Product: Penne Rigate Mozzarella Salad
Net Wt: 30 OZ (1 LB 14 OZ) 850 g
Packaging: Plastic container
Code: 3515-2
Use By Date: 06/1/23
The hazard
The product contains undeclared milk, which poses a risk to consumers with milk allergies. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show ASK Foods Inc has issued 10 other recalls since July 20, 2016. Recent brand recalls include an undeclared soy allergen recall on Dec. 16, 2025, and a metal pieces hazard recall on Jan. 7, 2020. Other recent recalls of similar products include Wawa Diet Iced Tea Lemon Pint Recall (April 2, 2026), Wawa Diet Lemonade P Recall (April 2, 2026), and Wawa Iced Tea Lemon Recall (April 2, 2026).
How to tell if you have this one
Check for the 3515-2 label on the product packaging. The product was sold with a use-by date of June 1, 2023.
Brand
Wegmans
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the 3515-2 label on the packaging to confirm it's the recalled item.
Where it went and when
Where it was distributed
Distributed in 3 states.
Listed by the agency
Not listed
FDA distribution: “Distributed to a distribution center in NY and then further distributed to stores in New York, Pennsylvania, and Massachusetts.” 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 5 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-0998-2023 (May 25, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0998-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.