Lifeforce Medical Institute Ultra Power — Class II food recall F-0179-2014
Terminated recall by ProThera, Inc., reported 2013-11-27. Firm was notified by supplier of the enzyme Xylanase that it was contaminated with chloramphenicol.
| Recall number | F-0179-2014 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | ProThera, Inc., Reno, NV, United States |
| Recall initiated | 2013-11-06 |
| Classified | 2013-11-18 |
| Reported by FDA | 2013-11-27 |
| Terminated | 2014-07-16 |
| Countries outside the US | CA, DE, ES, GB, HK, KR, MX, MY, PH, RU, SG |
| Quantity | 48,000 capsules |
Product
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
Reason for recall
Firm was notified by supplier of the enzyme Xylanase that it was contaminated with chloramphenicol.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-0179-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.