Food Recall Check
Class I · High risk Terminated Initiated Apr 5, 2014 (13 years ago)

TRADER GIOTTO'S CAESAR SALAD with Caesar Dressing recall

Recalled by H Group · Framingham, MA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Product labeling on Trader Giotto's Caesar Salad with Caesar Dressing may not list wheat, soy, egg and fish (anchovy) allergens.

Undeclared allergens: Egg Soy Wheat Fish

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

TRADER GIOTTO'S CAESAR SALAD with Caesar Dressing, NET WT. 8/5 OZ (241g).

Quantity: 509 units

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.

Sell by 4/6/14, 4/7/14, and 4/8/14.

Where it was sold

District of Columbia Delaware Maryland New Jersey New York Pennsylvania Virginia Washington

FDA's distribution note: Trader Joe's Stores in Delaware, Maryland, New Jersey, New York, Northern Virginia, Pennsylvania, and Washington, DC.

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 egg, soy, wheat, fish; 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
H Group
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 5, 2014
In FDA report of
May 21, 2014
Terminated
Feb 9, 2017
FDA recall number
F-1940-2014 · event 67946
Official record
FDA enforcement report search