Wish Bone House Italian Salad Dressing Recall: Unlabeled Milk and Egg
Pinnacle Food Group recalls Wish Bone House Italian Salad Dressing 15 oz. due to unlabeled milk and egg ingredients. Consumers should check product labels for the case lot code 4913019S51.
Lower-risk recall
The recall was initiated after learning from a retail customer that a limited number of bottles were mislabeled. The product contains milk and egg not declared on the bottle.
Contact the company
What happened, in plain English
Pinnacle Food Group is recalling a limited number of Wish Bone House Italian Salad Dressing bottles because they contain milk and egg that weren't listed on the label. This could affect people with allergies to milk or eggs who might unknowingly consume the product. Read more at govinfonow.com/recall/19017-wish-bone-house-italian-salad-dressing-recall-unlabeled-milk-and.
Source Summary by GovInfoNow · govinfonow.com/recall/19017-wish-bone-house-italian-salad-dressing-recall-unlabeled-milk-and · Updated October 6, 2026 · FDA enforcement record: FDA #F-1655-2018
Cite this page
“Wish Bone House Italian Salad Dressing Recall: Unlabeled Milk and Egg.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/19017-wish-bone-house-italian-salad-dressing-recall-unlabeled-milk-and. Based on FDA recall #F-1655-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1655-2018%22&limit=1).
Why it’s dangerous
The product contains milk and egg ingredients that were not declared on the bottle label. This could lead to allergic reactions in people who are sensitive or allergic to these ingredients.
Who’s affected
People who own or use Wish Bone House Italian Salad Dressing 15 oz. bottles with case lot code 4913019S51 are most at risk if they have milk or egg allergies. Others are less likely to be affected.
How to tell if you have this one
Check for the case lot code 4913019S51 on the bottle. The product is a 15 oz. Wish Bone House Italian Salad Dressing bottle.
- Brand
Pinnacle Food Group- Category
Food
What to do — step by step
Check Product Label
Look for the case lot code 4913019S51 on the bottle to confirm if it's recalled.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “73 locations received the product. The locations are a mix of retailers and distributors. Product was distributed nationwide to receiving locations in 31 states.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 3.4 years after the firm started it.
- Firm started the recall
- Published in FDA’s Enforcement Report
- FDA classified it Class I
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Is there a risk of serious injury from this product?
The recall is due to unlabeled milk and egg ingredients, which could cause allergic reactions in sensitive individuals. There is no mention of serious injury risk in normal use.
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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-1655-2018 (June 28, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1655-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 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.