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Class II: temporary or reversible health riskTerminated

ProThera Lifeforce Medical Institute Ultra Power Recall

Lifeforce Medical Institute Ultra Power

ProThera, Inc. · Reno, NV

Risk level
Class II
Reported by FDA
Nov 27, 2013
Recall ID
F-0179-2014
Check your lot numberHow we source this data

Summary

ProThera recalled Lifeforce Medical Institute Ultra Power starting Nov 6, 2013. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0179-2014 on Nov 27, 2013. Reason: Firm was notified by supplier of the enzyme Xylanase that it was contaminated with chloramphenicol. Status: Terminated.

Why it was recalled

Firm was notified by supplier of the enzyme Xylanase that it was contaminated with chloramphenicol.

Product description

Lifeforce Medical Institute Ultra Power; Optimal Vitamin/Mi neral. Trace Element/Anti-Oxidant Detox Support Dietary Supplement. 10 tablets/Packet and 30 packets/1000cc bottle. Distributed by: Mark Rosenbloom, MD LIFEFORCE Medical Institute 60 Revere Dr., Ste. 820 Northbrook, IL 60062 (847) 905-9505 www.lifeforcemed.com

Lot numbers, UPCs & expiration codes

361849A, Product code CT-80924A

Where it was sold

US and Canada, Germany, Great Britain, Hong Kong, Malaysia, Mexico, Philippines, Russia, Singapore, South Korea , Spain

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-0179-2014
Classification
Class II
Status
Terminated
Recall initiated
Nov 6, 2013
FDA report date
Nov 27, 2013
Quantity
48,000 capsules
Recall type
Voluntary: Firm initiated
Recalling firm
ProThera, Inc.

Original FDA data

Every field from FDA enforcement report F-0179-2014, exactly as published.

Show all FDA fields
City
Reno
State
NV
Status
Terminated
Country
United States
Event ID
66793
Address
10439 Double R Blvd
Code information
361849A, Product code CT-80924A
Postal code
89521-8905
Report date
Nov 27, 2013
Product type
Food
Recall number
F-0179-2014
Classification
Class II
Recalling firm
ProThera, Inc.
Product quantity
48,000 capsules
Termination date
Jul 16, 2014
Reason for recall
Firm was notified by supplier of the enzyme Xylanase that it was contaminated with chloramphenicol.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Lifeforce Medical Institute Ultra Power; Optimal Vitamin/Mi neral. Trace Element/Anti-Oxidant Detox Support Dietary Supplement. 10 tablets/Packet and 30 packets/1000cc bottle. Distributed by: Mark Rosenbloom, MD LIFEFORCE Medical Institute 60 Revere Dr., Ste. 820 Northbrook, IL 60062 (847) 905-9505 www.lifeforcemed.com
Distribution pattern
US and Canada, Germany, Great Britain, Hong Kong, Malaysia, Mexico, Philippines, Russia, Singapore, South Korea , Spain
Recall initiation date
Nov 6, 2013
Initial firm notification
Letter
Center classification date
Nov 18, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0179-2014, published Nov 27, 2013. View the source record (openFDA) · FDA enforcement reports

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

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