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Class IITerminated in FDA datasetRecall initiated Apr 2, 2013

Metabolic Whey - Vanilla¿5 LBS French Vanilla 10lbs: Whey Protein/Isolate, Soy Lecithin

Recalling firm: Chemi- Source Inc, Nutra Pak

Why it was recalled

Source of whey ingredient not listed as milk, an allergen; soy lecithin stated as "lecithin".Consumers who have an allergy or severe sensitivity to milk or soy run the risk of a…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Apr 15, 2014.

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Compare the exact product and package details with the label you have.

ProductMetabolic Whey - Vanilla¿5 LBS French Vanilla 10lbs: Whey Protein/Isolate, Soy Lecithin UPC 6-09492 72051-1 (VANILLA) UPC 6-09492 72054-2 (FRENCH VANILLA)
Package size5 LBS
UPC609492720511, 609492720542

FDA code information

expiration date between Jan 2013 and March 2016.

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Full FDA record and distribution details

Original product description

Metabolic Whey - Vanilla¿5 LBS French Vanilla 10lbs: Whey Protein/Isolate, Soy Lecithin UPC 6-09492 72051-1 (VANILLA) UPC 6-09492 72054-2 (FRENCH VANILLA)

Extracted codes and context

TypeCode / valueContext
UPC609492720511y - Vanilla¿5 LBS French Vanilla 10lbs: Whey Protein/Isolate, Soy Lecithin UPC 6-09492 72051-1 (VANILLA) UPC 6-09492 72054-2 (FRENCH VANILLA)
UPC609492720542a 10lbs: Whey Protein/Isolate, Soy Lecithin UPC 6-09492 72051-1 (VANILLA) UPC 6-09492 72054-2 (FRENCH VANILLA)

Original FDA recall reason

Source of whey ingredient not listed as milk, an allergen; soy lecithin stated as "lecithin".Consumers who have an allergy or severe sensitivity to milk or soy run the risk of a serious or life-threatening allergic reaction if they consume these products.

Recall details

Recall number
F-1495-2013
Event ID
64831
FDA status
Terminated
Initiated
Apr 2, 2013
Reported
Jun 12, 2013
Classified
Jun 6, 2013
Terminated
Apr 15, 2014
Quantity
5 # x 34,409 ; 10 # x 12,925
Location
Grand Rapids, MI, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

nationwide

FDA source record · F-1495-2013

Data updated September 16, 2026. View official FDA data ↗

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