Why it was recalled
Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Product description
CytoDetox, Hydrolyzed Clinoptilolite Fragments, 1 oz./30 mL, OTC Non-Sterile. Dietary supplement.
Lot numbers, UPCs & expiration codes
UPC No. 632687615989; Lot No. 30661601, Exp. Date 05/2018.
Where it was sold
FL, MI, MS, and OH.
What to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- F-0276-2017
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Aug 8, 2016
- FDA report date
- Nov 2, 2016
- Quantity
- 1,990 bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Pharmatech LLC
Original FDA data
Every field from FDA enforcement report F-0276-2017, exactly as published.
Show all FDA fields
- City
- Davie
- State
- FL
- Status
- Terminated
- Country
- United States
- Event ID
- 75272
- Address
- 4131 SW 47th Ave Ste 1403
- Code information
- UPC No. 632687615989; Lot No. 30661601, Exp. Date 05/2018.
- Postal code
- 33314-4036
- Report date
- Nov 2, 2016
- Product type
- Food
- Recall number
- F-0276-2017
- Classification
- Class II
- Recalling firm
- Pharmatech LLC
- Product quantity
- 1,990 bottles
- Termination date
- Sep 23, 2024
- Reason for recall
- Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- CytoDetox, Hydrolyzed Clinoptilolite Fragments, 1 oz./30 mL, OTC Non-Sterile. Dietary supplement.
- Distribution pattern
- FL, MI, MS, and OH.
- Recall initiation date
- Aug 8, 2016
- Initial firm notification
- Letter
- Center classification date
- Oct 25, 2016