FDA recall record
Poly-Vita Drops, 50 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
Poly-Vita Drops, 50 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.
Poly-Vita Drops, 50 mL, OTC Non-Sterile. Dietary supplement.
Code information listed by FDA
NDC No. 0904-5099-50; Lot No. 20701509 & 20701511, Exp. Date 09/2017; Lot No. 20701513, Exp. Date 12/2017; Lot No. 20701601, Exp. Date 02/2018; Lot No. 20701602 & 20701603, Exp. Date 04/2018; Lot No. 20701606, Exp. Date 06/2016.
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: 42,984 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.