Pharmatech Recalls CytoDetox Supplement Due to Potential Bacterial Contamination
Pharmatech LLC is recalling 1,990 bottles of CytoDetox dietary supplement due to a precautionary measure regarding potential contamination with Burkholderia cepacia.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is explicitly described as a precautionary measure with no reported illnesses or injuries, which aligns with the rubric for voluntary precautionary recalls.
Plain-English summary
Pharmatech LLC is recalling 1,990 bottles of CytoDetox, Hydrolyzed Clinoptilolite Fragments, 1 oz./30 mL, OTC Non-Sterile dietary supplement. The recall was initiated as a precautionary measure due to the potential risk of product contamination with Burkholderia cepacia.
The affected product is identified by UPC No. 632687615989, Lot No. 30661601, and an expiration date of 05/2018. The product was distributed in Florida, Michigan, Mississippi, and Ohio.
Consumers who purchased this product should stop using it and contact Pharmatech LLC for further instructions.
The recalled product
- Product
- CytoDetox, Hydrolyzed Clinoptilolite Fragments, 1 oz./30 mL, OTC Non-Sterile. Dietary supplement.
- Manufacturer
- Pharmatech LLC
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 1,990
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- UPC No. 632687615989
- Lot No. 30661601
- Exp. Date 05/2018.
Distribution
Part of a larger recall action
This product is one of 23 recalled by Pharmatech LLC under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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