Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported November 27, 2013
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
Firm was notified by supplier of the enzyme Xylanase that it was contaminated with chloramphenicol.
Compiled from official public sources by the editorial team.
Verify with FDA Food →
ProThera, Inc. recalled Lifeforce Medical Institute Ultra Power; Optimal Vitamin/Mi neral. Trace Element/Anti-Ox… - a moderate-severity action.
Lifeforce Medical Institute Ultra Power; Optimal Vitamin/Mi neral. Trace Element/Anti-Ox… was recalled by ProThera, Inc. in November 27, 2013. Reason: Firm was notified by supplier of the enzyme Xylanase that it was contaminated with chloramphenicol.. Check the official notice for the remedy. Verify recall #F-0179-2014 with the FDA Food before acting.
The recall
ProThera, Inc. issued this moderate-severity FDA Food recall-Firm was notified by supplier of the enzyme Xylanase that it was contaminated with chloramphenicol..
- Moderate
- severity level
- Class II
- classification
- November 27, 2013
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0179-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-0179-2014) was formally reported on November 27, 2013, with the manufacturer initiating the action on November 6, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. ProThera, Inc. is listed as the recalling firm, operating out of Reno, NV. Federal records list the affected scope as 48,000 capsules.
The documented reason for this recall is: Firm was notified by supplier of the enzyme Xylanase that it was contaminated with chloramphenicol. Distribution data in the federal record shows the product reached: US and Canada, Germany, Great Britain, Hong Kong, Malaysia, Mexico, Philippines, Russia, Singapore, South Korea , Spain. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,731 children & baby products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
48,000 capsules
Related Recalls
6
0 from same agency
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
Reason for recall
Firm was notified by supplier of the enzyme Xylanase that it was contaminated with chloramphenicol.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-0179-2014 |
| Date reported | November 27, 2013 |
| Date initiated | November 6, 2013 |
| Recalling firm | ProThera, Inc. |
| Firm location | Reno, NV |
| Affected scope | 48,000 capsules |
| Distribution | US and Canada, Germany, Great Britain, Hong Kong, Malaysia, Mexico, Philippines, Russia, Singapore, South Korea , Spain |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-0179-2014) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by ProThera, Inc.. Units affected: 48,000 capsules.
Why was this product recalled? ▼
Firm was notified by supplier of the enzyme Xylanase that it was contaminated with chloramphenicol.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on November 27, 2013. Severity: Moderate. Recall number: F-0179-2014.
Where was the recalled product distributed? ▼
Distribution: US and Canada, Germany, Great Britain, Hong Kong, Malaysia, Mexico, Philippines, Russia, Singapore, South Korea , Spain.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0179-2014) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported November 27, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.