Recall · openFDA Food Enforcement
Poly-Vita Drops, 50 mL, OTC Non-Sterile. Dietary supplement.: FDA Recall F-0266-2017 Agency action: Aug 8, 2016 Record ID: F-0266-2017
View official source ↗ What happened Original notice title
Poly-Vita Drops, 50 mL, OTC Non-Sterile. Dietary supplement., recall F-0266-2017
From the archived source record
Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
What the official notice says to do Check the original notice for the instructions that apply to the named product, company, and affected lots.
Read the official notice → Status and source details
Status recorded in the archive Terminated
FDA recall classification Class II
Recall initiated by Voluntary: Firm initiated
Report date Nov 2, 2016
Termination date in the archive Sep 23, 2024
Source checked Jul 16, 2026
Record revision 7d74a106e95b This is a dated record. Its current status may have changed since the source was captured. A record applies to its stated scope; it is not a safety rating for every product from a company.
Sources, dates, and coverage → What is affected Product Poly-Vita Drops, 50 mL, OTC Non-Sterile. Dietary supplement. Company Pharmatech LLC Lot / identifier 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. Market / distribution FL, MI, MS, and OH. Quantity reported 42,984 bottles What is affected Product Poly-Vita Drops, 50 mL, OTC Non-Sterile. Dietary supplement. Company Pharmatech LLC Lot / identifier 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. Market / distribution FL, MI, MS, and OH. 