Birds Eye Baby Sweet Peas
Reason Product has the potential to be contaminated with Listeria monocytogenes.
Wish Bone House Italian Salad Dressing recall
Recalled by Pinnacle Food Group, Llc · Cherry Hill, NJ, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
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.
Undeclared allergens: Milk Egg
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
Wish Bone House Italian Salad Dressing 15 oz.
Quantity: 7,768 cases
Food: Sauces, dips & dressings
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Item number 004132100648 Case Lot Code 4913019S51
Where it was sold
Nationwide.
FDA's distribution note: 73 locations received the product. The locations are a mix of retailers and distributors. Product was distributed nationwide to receiving locations in 31 states.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to milk, egg; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Pinnacle Food Group, Llc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 28, 2018
- In FDA report of
- Jul 18, 2018
- Terminated
- Nov 17, 2021
- FDA recall number
- F-1655-2018 · event 80405
- Official record
- FDA enforcement report search
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