Gerber Pasta Pick-Ups Cheese Ravioli Recall: Missing Egg Allergen Label
Gerber recalls Pasta Pick-Ups Cheese Ravioli due to missing egg allergen label. Consumers should check product codes and contact Gerber for details.
Lower-risk recall
Gerber Products Company is recalling Cheese Ravioli Gerber¿ Pasta Pick-Ups¿ because the egg allergen is missing from the "Contains" statement.
Contact the company
What happened, in plain English
Gerber is recalling Pasta Pick-Ups Cheese Ravioli because the product's label does not list eggs as an allergen. This could affect people with egg allergies who might consume the product without knowing. Read more at govinfonow.com/recall/22022-gerber-pasta-pick-ups-cheese-ravioli-recall-missing-egg-allergen.
Source Summary by GovInfoNow · govinfonow.com/recall/22022-gerber-pasta-pick-ups-cheese-ravioli-recall-missing-egg-allergen · Updated October 8, 2026 · FDA enforcement record: FDA #F-1922-2017
Cite this page
“Gerber Pasta Pick-Ups Cheese Ravioli Recall: Missing Egg Allergen Label.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22022-gerber-pasta-pick-ups-cheese-ravioli-recall-missing-egg-allergen. Based on FDA recall #F-1922-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1922-2017%22&limit=1).
Why it’s dangerous
The product label does not list eggs as an allergen, which could lead to allergic reactions in infants who are sensitive to eggs. This is a labeling issue, not a physical defect in the product.
Who’s affected
Parents and caregivers of infants who have egg allergies are most at risk. The recall affects specific product codes sold in the U.S.
How to tell if you have this one
Check for the UPC code 01500000907-6 on the package. The product is sold in the U.S. and is labeled as 'Pasta Pick-Ups Cheese Ravioli Net Wt 6 oz (170g) Drained Wt 3 oz (85g)'.
- Brand
Gerber- Product
Gerber¿ Pasta Pick-Ups Cheese Ravioli Net Wt 6 oz (170g) Drained Wt 3 oz (85g) UPC 01500000907-6 , Truncated - written- Category
Food
What to do — step by step
Check Product Label
Look for the UPC code 01500000907-6 on the package to confirm it is the recalled item.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 11 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-1922-2017 (March 8, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1922-2017 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.