PGP International iForce Nutrition Xtreme Series Recall

Why it was recalled

The product contains undeclared wheat.

Product description

iForce Nutrition Xtreme Series, PROTEAN, Lean Protein, Strawberry Creamsicle, Dietary Supplement, 4 lbs. Mfg. for Dist by, Tribravus Enterprises, LLC, Vista, CA 92081

Lot numbers, UPCs & expiration codes

Lot # SP1327D2, Exp. 11/23/2013; Lot # SP 1349B2, Exp. 12/15/2013 and Lot # SP 2072B2, Exp. 03/12/2014

Where it was sold

The product has been distributed in CA, NC and WI.

What to do if you have this product

Compare the brand, size, and lot/UPC codes on your package with the codes above.
If it matches, don't eat it. Return it to the store for a refund or throw it away.
Wash surfaces and containers that touched the product.
If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number: F-1654-2012
Classification: Class II
Status: Terminated
Recall initiated: Jun 11, 2012
FDA report date: Jul 4, 2012
Quantity: 1,616/ 4 lb-bottles
Recall type: Voluntary: Firm initiated
Recalling firm: PGP International, Inc.

Original FDA data

Every field from FDA enforcement report F-1654-2012, exactly as published.

Show all FDA fields

City: Springfield
State: MO
Status: Terminated
Country: United States
Event ID: 62292
Address: 1904 N Lecompte Rd bldg #15
Address (line 2): Po Box 1247
Code information: Lot # SP1327D2, Exp. 11/23/2013; Lot # SP 1349B2, Exp. 12/15/2013 and Lot # SP 2072B2, Exp. 03/12/2014
Postal code: 65802
Report date: Jul 4, 2012
Product type: Food
Recall number: F-1654-2012
Classification: Class II
Recalling firm: PGP International, Inc.
Product quantity: 1,616/ 4 lb-bottles
Termination date: Dec 19, 2012
Reason for recall: The product contains undeclared wheat.
Voluntary / mandated: Voluntary: Firm initiated
Product description: iForce Nutrition Xtreme Series, PROTEAN, Lean Protein, Strawberry Creamsicle, Dietary Supplement, 4 lbs. Mfg. for Dist by, Tribravus Enterprises, LLC, Vista, CA 92081
Distribution pattern: The product has been distributed in CA, NC and WI.
Recall initiation date: Jun 11, 2012
Initial firm notification: E-Mail
Center classification date: Jun 25, 2012

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1654-2012, published Jul 4, 2012. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

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