Food Recall Check
Class I · High risk Terminated Initiated Jul 5, 2017 (9 years ago)

Clif Kid Zbar Protein Chocolate Mint 10-pack recall

Recalled by Clif Bar & Company · Emeryville, CA, United States

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

Why it was recalled

Undeclared peanuts and/or tree nuts.

Undeclared allergens: Peanut Tree nuts

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

Clif Kid Zbar Protein Chocolate Mint 10-pack, 150-count, 5-pack;

Quantity: 100,685,754 total

Food: Chocolate & candy

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 Code From 05APR16M3 to 23APR18M3

Where it was sold

Nationwide.

FDA's distribution note: Nationwide. distribution and to United Kingdom, and Ireland.

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 peanut, tree nuts; 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
Clif Bar & Company
Initiated by
Voluntary: Firm initiated
Recall initiated
Jul 5, 2017
In FDA report of
Aug 9, 2017
Terminated
Feb 14, 2019
FDA recall number
F-2963-2017 · event 77700
Official record
FDA enforcement report search

Also recalled with it (4 more products)

FDA files each product of one recall action separately; these share the same FDA event.

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