CLASS I Food recall · Reported 27 Mar 2013 · FDA Enforcement Report

Dymatize Nutrition Xpand Post Xtreme Mass Recovery System recalled

Dymatize Enterprises is recalling Dymatize Nutrition Xpand Post Xtreme Mass Recovery System Lemonade Manufactured, distributed in Puerto Rico. The recall was initiated on 3 May 2012 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLots 1244001, 1292001, 1021101, 1075102, and 1276102.
Quantity recalled9,962 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1229-2013
FDA event ID
61735
Recalling firm
Dymatize Enterprises, Farmers Branch, TX
Classification
Class I
Status
Terminated
Recall initiated
3 May 2012
FDA classified
18 Mar 2013
Reported
27 Mar 2013
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Milk
Product category
Juice

Timeline

3 May 2012Recall initiated by company
18 Mar 2013Classified by FDA+319 days
27 Mar 2013Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

The product label declares whey but does not declare milk.

Product as listed by the FDA

Dymatize Nutrition XPAND Post Xtreme Mass Recovery System Lemonade 3.5 lb Manufactured & Distributed by Dymatize Enterprises, LLC, 13737 N. Stemmons FWY. Dallas, TX 75234 UPC 705016895649

Where it was distributed

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.

Puerto Rico

Questions about this recall

Why was it recalled?

The product label declares whey but does not declare milk.

Which lots are affected?

Lots 1244001, 1292001, 1021101, 1075102, and 1276102.

Where was it sold?

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.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

2 other products · FDA event 61735

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