FDA recall record
Cerovite Liquid, 8 oz./236 mL, OTC Non-Sterile. Dietary supplement.
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of September 23, 2024. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
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.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Cerovite Liquid, 8 oz./236 mL, OTC Non-Sterile. Dietary supplement.
Code information listed by FDA
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.
Distribution and firm information
Recalling firm listed by FDA: Pharmatech LLC
Firm location listed by FDA: Davie, FL, United States
Distribution reported by FDA: FL, MI, MS, and OH.
Product quantity listed by FDA: 129,268 bottles
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.