MRM All Natural Whey - Dutch Chocolate 2.02 lbs, 1.01 lbs; All Natural Whey 10pk/bx Dutch…
Recalling firm: Chemi- Source Inc, Nutra Pak
Source of whey ingredient not listed as milk, an allergen. Consumers who have an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic…
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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609492720047, 609492720054, 609492720955FDA code information
expiration date between Jan 2013 and March 2016. ;
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Full FDA record and distribution details
Original product description
MRM All Natural Whey - Dutch Chocolate 2.02 lbs, 1.01 lbs; All Natural Whey 10pk/bx Dutch Chocolate: Whey Protein/Isolate Contains: Soy, Dairy, Cocoa, Nitrozyme UPC 6-09492 72004-7 (2.02 lbs) UPC 6-09492 72095-5 (10 pk) UPC 6-09492 72005-4(1.01 lbs)
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 609492720047 | utch Chocolate: Whey Protein/Isolate Contains: Soy, Dairy, Cocoa, Nitrozyme UPC 6-09492 72004-7 (2.02 lbs) UPC 6-09492 72095-5 (10 pk) UPC 6-09492 72005-4(1.01 lbs) |
| UPC | 609492720054 | coa, Nitrozyme UPC 6-09492 72004-7 (2.02 lbs) UPC 6-09492 72095-5 (10 pk) UPC 6-09492 72005-4(1.01 lbs) |
| UPC | 609492720955 | late Contains: Soy, Dairy, Cocoa, Nitrozyme UPC 6-09492 72004-7 (2.02 lbs) UPC 6-09492 72095-5 (10 pk) UPC 6-09492 72005-4(1.01 lbs) |
Original FDA recall reason
Source of whey ingredient not listed as milk, an allergen. Consumers who have an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume these products.
Recall details
- Recall number
- F-1498-2013
- Event ID
- 64831
- FDA status
- Terminated
- Initiated
- Apr 2, 2013
- Reported
- Jun 12, 2013
- Classified
- Jun 6, 2013
- Terminated
- Apr 15, 2014
- Quantity
- 2.02 # x 136726; 1.01 # x 49,235; 10 pak x 42,699
- Location
- Grand Rapids, MI, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Telephone
Where it was distributed
nationwide
Data updated September 16, 2026. View official FDA data ↗
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