Cerovite Liquid
Recalling firm: Pharmatech LLC
Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Sep 23, 2024.
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FDA code information
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.
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Full FDA record and distribution details
Original product description
Cerovite Liquid, 8 oz./236 mL, OTC Non-Sterile. Dietary supplement.
Original FDA recall reason
Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Recall details
- Recall number
- F-0258-2017
- Event ID
- 75272
- FDA status
- Terminated
- Initiated
- Aug 8, 2016
- Reported
- Nov 2, 2016
- Classified
- Oct 25, 2016
- Terminated
- Sep 23, 2024
- Quantity
- 129,268 bottles
- Location
- Davie, FL, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was distributed
FL, MI, MS, and OH.
Data updated September 16, 2026. View official FDA data ↗
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