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Class II: temporary or reversible health riskTerminated

Protica ProBalance Protein To Go(TM) Recall

ProBalance Protein To Go(TM), Caffeinated French Vanilla Latte, Dietary Supplement

Protica, Inc · Whitehall, PA

Risk level
Class II
Reported by FDA
Sep 26, 2012
Recall ID
F-2350-2012
Check your lot numberHow we source this data

Summary

Protica recalled ProBalance Protein To Go(TM) starting Aug 17, 2012. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-2350-2012 on Sep 26, 2012. Reason: Product not sufficiently acidified (equilibrium pH higher than 4.6), therefore it has the potential to be contaminated with Clostridium botulinum. Status: Terminated.

Why it was recalled

Product not sufficiently acidified (equilibrium pH higher than 4.6), therefore it has the potential to be contaminated with Clostridium botulinum

Product description

ProBalance Protein To Go(TM), Caffeinated French Vanilla Latte, Dietary Supplement, Net Wt 2.5 fl oz (Responsible firm on labeling: Pro Balance LLC, 4070 Tampa Road, Oldsmar, FL 34677)

Lot numbers, UPCs & expiration codes

Lot numbers PP25114066A, PP25114066B, PP28414079, PP29114086, PP34014103, PP04424112, PP09324122, PP09524125, PP10224129, PP11524133A, PP11524133B, PP11524133C, PP12224138A, PP12224138B, PP12224138, PP12924141, PP15924146A, and PP16024146B.

Where it was sold

Nationwide distribution - product was distributed to direct accounts in AL, AZ, FL, IL, IN, KY, MN, MO, MS, NY OH, OK, RI, SC, TX and VA.

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-2350-2012
Classification
Class II
Status
Terminated
Recall initiated
Aug 17, 2012
FDA report date
Sep 26, 2012
Quantity
230,000 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Protica, Inc

Original FDA data

Every field from FDA enforcement report F-2350-2012, exactly as published.

Show all FDA fields
City
Whitehall
State
PA
Status
Terminated
Country
United States
Event ID
62962
Address
1002 Macarthur Rd
Code information
Lot numbers PP25114066A, PP25114066B, PP28414079, PP29114086, PP34014103, PP04424112, PP09324122, PP09524125, PP10224129, PP11524133A, PP11524133B, PP11524133C, PP12224138A, PP12224138B, PP12224138, PP12924141, PP15924146A, and PP16024146B.
Postal code
18052
Report date
Sep 26, 2012
Product type
Food
Recall number
F-2350-2012
Classification
Class II
Recalling firm
Protica, Inc
Product quantity
230,000 bottles
Termination date
Jun 9, 2015
Reason for recall
Product not sufficiently acidified (equilibrium pH higher than 4.6), therefore it has the potential to be contaminated with Clostridium botulinum
Voluntary / mandated
Voluntary: Firm initiated
Product description
ProBalance Protein To Go(TM), Caffeinated French Vanilla Latte, Dietary Supplement, Net Wt 2.5 fl oz (Responsible firm on labeling: Pro Balance LLC, 4070 Tampa Road, Oldsmar, FL 34677)
Distribution pattern
Nationwide distribution - product was distributed to direct accounts in AL, AZ, FL, IL, IN, KY, MN, MO, MS, NY OH, OK, RI, SC, TX and VA.
Recall initiation date
Aug 17, 2012
Initial firm notification
Telephone
Center classification date
Sep 19, 2012

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-2350-2012, published Sep 26, 2012. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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