Food Recall Check
Class I · High risk Terminated Initiated May 3, 2012 (14 years ago)

Dymatize Nutrition XPAND Post Xtreme Mass Recovery System Blue Raspberry recall

Recalled by Dymatize Enterprises, LLC · Farmers Branch, TX, United States

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

Why it was recalled

The product label declares whey but does not declare milk.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

Dymatize Nutrition XPAND Post Xtreme Mass Recovery System Blue Raspberry 3.5 lb Manufactured & Distributed by Dymatize Enterprises, LLC, 13737 N. Stemmons FWY. Dallas, TX 75234 UPC 705016895601.

Quantity: 9,983 units

Food: Berries

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.

Lots 1292004, 1244004, 1025102, 1075115, and 1153101.

Where it was sold

Puerto Rico

FDA's distribution note: Product was distributed in the United States, Algeria, Australia, Bulgaria, Canada, Cyprus, Czech Republic, Dominican Republic, France, French Polynesia, Germany, Indonesia, Italy, Jordan, Korea, Mexico, Netherlands, Philipines, Portugal, Puerto Rico, Qatar, Russia, Slovenija, South Africa, Spain, Sweden, Switzerland, Thailand, Turkey, and United Kingdom.

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. 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
Dymatize Enterprises, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
May 3, 2012
In FDA report of
Mar 27, 2013
Terminated
Oct 8, 2014
FDA recall number
F-1231-2013 · event 61735
Official record
FDA enforcement report search

Also recalled with it (2 more products)

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

Recent berries recalls

All berries recalls
Class II · Moderate risk Ongoing Foreign material

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Reason Flexible food pouch may release thin plastic strips into food.

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