Wegmans Ravioli Recall: Plastic Pieces in Product
Wegmans recalls Italian Classics Ravioli due to possible white plastic pieces. Consumers should check UPC 0-77890-38934 and stop using if found.
Lower-risk recall
Product may contain pieces of white plastic.
Contact the company
What happened, in plain English
Wegmans is recalling Italian Classics Ravioli that may contain white plastic pieces. This could cause injury if ingested. The product was sold in Wegmans stores from August 2-30, 2016. Read more at govinfonow.com/recall/23329-wegmans-ravioli-recall-plastic-pieces-in-product.
Source Summary by GovInfoNow · govinfonow.com/recall/23329-wegmans-ravioli-recall-plastic-pieces-in-product · Updated October 9, 2026 · FDA enforcement record: FDA #F-0042-2017
Cite this page
“Wegmans Ravioli Recall: Plastic Pieces in Product.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23329-wegmans-ravioli-recall-plastic-pieces-in-product. Based on FDA recall #F-0042-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0042-2017%22&limit=1).
Why it’s dangerous
The ravioli may contain small white plastic pieces that could be ingested. If swallowed, these pieces might cause choking or internal injury. The hazard is low risk as the plastic pieces are small and not likely to cause serious harm.
Who’s affected
Wegmans customers who bought the Italian Classics Ravioli with UPC 0-77890-38934 between August 2-30, 2016. Children and those with sensitive digestive systems are at slightly higher risk.
How to tell if you have this one
Check for the UPC 0-77890-38934 on the ravioli packaging. The product was sold in Wegmans stores from August 2 to August 30, 2016. The ravioli should be kept refrigerated until the use-by date of September 30, 2016.
- Brand
Wegmans- Product
Wegmans ITALIAN CLASSICS RICOTTA & SPINACH STRIPED JUMBO RAVIOLI, NET WT 9 OZ. (255g), UPC 0-77890-38934, KEEP- Category
Food
What to do — step by step
Check for Plastic Pieces
Inspect the ravioli for small white plastic pieces before eating.
Where it went and when
Where it was distributed
Distributed in 6 states.
FDA distribution: “New York, New Jersey, Pennsylvania, Virginia, Maryland, and Massachusetts” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Maryland, Massachusetts, New Jersey, New York, Pennsylvania, Virginia.
Recall timeline
FDA terminated this recall 21 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- 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-0042-2017 (September 2, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0042-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 9, 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.