Severity
Moderate
FDA Food recall · Reported November 20, 2013
ProThera was notified by enzymes provided by Specialty Enzymes within the last 3-6 months may be contaminated with chloramphenicol.
ProThera, Inc. recalled Klaire Labs Vital-Zymes complete; Comprehensive Enzyme Supplement; 120 Vegetarian table… - a moderate-severity action.
Klaire Labs Vital-Zymes complete; Comprehensive Enzyme Supplement; 120 Vegetarian table… was recalled by ProThera, Inc. in November 20, 2013. Reason: ProThera was notified by enzymes provided by Specialty Enzymes within the last 3-6 months may be contaminated…. Check the official notice for the remedy. Verify recall #F-0160-2014 with the FDA Food before acting.
The recall
ProThera, Inc. issued this moderate-severity FDA Food recall-ProThera was notified by enzymes provided by Specialty Enzymes within the last 3-6 months may be contaminated….
Sourced from official FDA Food enforcement records. Verify recall #F-0160-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-0160-2014) was formally reported on November 20, 2013, with the manufacturer initiating the action on October 10, 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 187,941 lot 0613110; 491.232 lot 0513156 and 504864 lot 0513157.
The documented reason for this recall is: ProThera was notified by enzymes provided by Specialty Enzymes within the last 3-6 months may be contaminated with chloramphenicol. Distribution data in the federal record shows the product reached: US and Australia, Azerbaijan, Brazil, Canada, Germany, Great Britain, Hong Kong, Ireland (Eire, Japan, Malaysia, Malta, Mexico, New Zealand, Panama, Philippines, Russia, South Korea, Spain, Switzerland, Thailand.. 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, 6 from FDA Food - 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.
Where this recall sits in its category - 2,002 dietary supplements 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.
Severity
Moderate
Affected scope
187,941 lot 0613110; 491.232 lot 0513156 and 504864 lot 0513157
Related Recalls
6
6 from same agency
Klaire Labs Vital-Zymes complete; Comprehensive Enzyme Supplement; 120 Vegetarian tablets. UPC 790616310005 Manufactured by ProThera, Inc., , Klaire Labs is a division of ProThera Reno, NV 89521
ProThera was notified by enzymes provided by Specialty Enzymes within the last 3-6 months may be contaminated with chloramphenicol.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-0160-2014 |
| Date reported | November 20, 2013 |
| Date initiated | October 10, 2013 |
| Recalling firm | ProThera, Inc. |
| Firm location | Reno, NV |
| Affected scope | 187,941 lot 0613110; 491.232 lot 0513156 and 504864 lot 0513157 |
| Distribution | US and Australia, Azerbaijan, Brazil, Canada, Germany, Great Britain, Hong Kong, Ireland (Eire, Japan, Malaysia, Malta, Mexico, New Zealand, Panama, Philippines, Russia, South Korea, Spain, Switzerland, Thailand. |
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.
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.
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 20, 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.