CLASS II Food recall · Reported 20 Nov 2013 · FDA Enforcement Report
Klaire Labs Vital-Zymes complete recalled by ProThera
ProThera is recalling Klaire Labs Vital-Zymes complete. The recall was initiated on 10 Oct 2013 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0160-2014
- FDA event ID
- 66553
- Recalling firm
- ProThera, Reno, NV
- Brand
- Klaire Labs
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 10 Oct 2013
- FDA classified
- 12 Nov 2013
- Reported
- 20 Nov 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Product category
- Dietary Supplements
Timeline
| 10 Oct 2013 | Recall initiated by company | |
| 12 Nov 2013 | Classified by FDA | +33 days |
| 20 Nov 2013 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
ProThera was notified by enzymes provided by Specialty Enzymes within the last 3-6 months may be contaminated with chloramphenicol.
Product as listed by the FDA
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
Where it was distributed
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.
Questions about this recall
Why was it recalled?
ProThera was notified by enzymes provided by Specialty Enzymes within the last 3-6 months may be contaminated with chloramphenicol.
Which lots are affected?
Lot #'s 0613110, 0513156 and 0513157
Where was it sold?
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.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
4 other products · FDA event 66553This product is part of a recall event; the main page for the event is Klaire Labs Interfase recalled by ProThera.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Klaire Labs Interfase recalled by ProTheraKlaire Labs | ProThera | Packaging Defects | NV | |
| CLASS II | Klaire Labs Vital-Zymes Chewable recalled by ProTheraKlaire Labs | ProThera | Other | NV | |
| CLASS II | Klaire Labs Interfase Plus recalled by ProTheraKlaire Labs | ProThera | Other | NV | |
| CLASS II | Serralase Enzyme Supplements recalled by ProTheraSerralase Enzyme | ProThera | Packaging Defects | NV |
More recalls from ProThera
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|---|---|---|---|---|---|
| Food | CLASS II | Klaire Labs Reduced L-Glutathione, single capsule dose recalledKlaire Labs | ProThera | Packaging Defects | 14 states |
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| Food | CLASS II | Klaire Labs Ther-Biotic Factor 6 100+ Billion Cfu's recalled by ProTheraKlaire Labs | ProThera | Foreign Material | Nationwide |
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| Food | CLASS II | Pro Thera Dual Detox Dietary Supplement;; Chlorella recalledPro Thera | ProThera | Other | NV |
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