Lifeforce Medical Institute Ultra Power; Optimal Vitamin/Mi neral. Trace Element/Anti-Oxidant…
Recalling firm: ProThera, Inc.
Firm was notified by supplier of the enzyme Xylanase that it was contaminated with chloramphenicol.
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: Jul 16, 2014.
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FDA code information
361849A, Product code CT-80924A
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Full FDA record and distribution details
Original 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
Original FDA recall reason
Firm was notified by supplier of the enzyme Xylanase that it was contaminated with chloramphenicol.
Recall details
- Recall number
- F-0179-2014
- Event ID
- 66793
- FDA status
- Terminated
- Initiated
- Nov 6, 2013
- Reported
- Nov 27, 2013
- Classified
- Nov 18, 2013
- Terminated
- Jul 16, 2014
- Quantity
- 48,000 capsules
- Location
- Reno, NV, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was distributed
US and Canada, Germany, Great Britain, Hong Kong, Malaysia, Mexico, Philippines, Russia, Singapore, South Korea , Spain
Data updated September 16, 2026. View official FDA data ↗
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