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Pharmatech LLC
FDA recall F-0258-2017 · Class II · reported 2016-11-02 · Terminated
- Product
- Cerovite Liquid, 8 oz./236 mL, OTC Non-Sterile. Dietary supplement.
- Reason
- Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
- Quantity
- 129,268 bottles
- Distribution
- FL, MI, MS, and OH.
- Firm location
- FL, United States
- Initiated
- Voluntary: Firm initiated
- First notice
- Letter
- Recall started
- 2016-08-08
- Terminated
- 2024-09-23
- Code info
- UPC No. 005362790590; Lot No. 20471516, 20471517, 20471518, 20471519, & 20471520, Exp. Date 11/2017; Lot No. 20471521, Exp. Date 12/2017; Lot No. 20471601, Exp. Date 01/2018; Lot No. 20471608, Exp. Date 04/2018; Lot No. 20471610 & 20471613, Exp. Date 05/2018; Lot No. 20471614, Exp. Date 06/2018.
Source: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.