CLASS II Food recall · Reported 27 Nov 2013 · FDA Enforcement Report
Pro Thera Dual Detox Dietary Supplement;; Chlorella - 500 mg recalled
ProThera is recalling Pro Thera Dual Detox Dietary Supplement;; Chlorella - 500 mg. The recall was initiated on 6 Nov 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-0180-2014
- FDA event ID
- 66793
- Recalling firm
- ProThera, Reno, NV
- Brand
- Pro Thera
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 6 Nov 2013
- FDA classified
- 18 Nov 2013
- Reported
- 27 Nov 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Product category
- Broccoli
Timeline
| 6 Nov 2013 | Recall initiated by company | |
| 18 Nov 2013 | Classified by FDA | +12 days |
| 27 Nov 2013 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Firm was notified by supplier of the enzyme Xylanase that it was contaminated with chloramphenicol.
Product as listed by the FDA
Pro Thera Dual Detox Dietary Supplement; 60 capsules; Chlorella - 500 mg; Broccoli Sprout, dried extract - 60 mg; Enzyme Blend - supplying Beta-Glucanase, Cellulase, Protease, Hemicellulase, Phytase and Xylanase Manufactured by ProThera, Reno, NV,
Where it was distributed
US and Canada, Germany, Great Britain, Hong Kong, Malaysia, Mexico, Philippines, Russia, Singapore, South Korea , Spain
Questions about this recall
Is Pro Thera Dual Detox Dietary Supplement;; Chlorella - 500 mg recalled?
Yes. ProThera recalled Pro Thera Dual Detox Dietary Supplement;; Chlorella - 500 mg on 6 Nov 2013. The recall is Class II and its status is Terminated. Recall number F-0180-2014.
Why was it recalled?
Firm was notified by supplier of the enzyme Xylanase that it was contaminated with chloramphenicol.
Which lots are affected?
Lot B3222, product code DTX
Where was it sold?
US and Canada, Germany, Great Britain, Hong Kong, Malaysia, Mexico, Philippines, Russia, Singapore, South Korea , Spain
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 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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