Food Recall Check
Class I · High risk Terminated Initiated Jul 20, 2015 (11 years ago)

CiCi's Cavatappi Enriched Macaroni Product recall

Recalled by ConAgra Foods Inc · Omaha, NE, United States

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

Why it was recalled

Undeclared egg. Egg containing-macaroni was inadvertently mixed with macaroni that did not contain egg.

Undeclared allergen: 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

CiCi's Cavatappi, Enriched Macaroni Product, packaged in 5-lb. bags, 4 bags per case, Packed exclusively for use by CiCi's Pizza and its Franchisees, JMC Restaurant Distribution, LP, Coppell, TX.

Quantity: Lot 063015V - 540/4/5-lb. bag cases; lot 070115V - 330/4/5-lb. bag cases

Food: Pasta, rice & grains

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.

Lot number 063015V, exp. June 30, 2017; and lot number 070115V, exp. July 1, 2017.

Where it was sold

Texas

FDA's distribution note: The product was distributed to one consignee in Texas. There was no foreign, government, nor military distribution.

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; 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
ConAgra Foods Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Jul 20, 2015
In FDA report of
Oct 7, 2015
Terminated
Apr 13, 2016
FDA recall number
F-3249-2015 · event 71938
Official record
FDA enforcement report search

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