Recall · openFDA Food Enforcement

D-Vita Drops, 50 mL, OTC Non-Sterile. Dietary supplement.: FDA Recall F-0268-2017

Agency action: Aug 8, 2016Record ID: F-0268-2017
View official source ↗

What happened

Original notice title

D-Vita Drops, 50 mL, OTC Non-Sterile. Dietary supplement., recall F-0268-2017

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
63862f64d66d

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
D-Vita Drops, 50 mL, OTC Non-Sterile. Dietary supplement.
Company
Pharmatech LLC
Lot / identifier
NDC No. 0904-6273-50; Lot No. 20691509, Exp. Date 11/2017; Lot No. 20691510, Exp. Date 12/2017; Lot No. 206916603, Exp. Date 03/2018; Lot No. 20691605, Exp. Date 04/2018.
Market / distribution
FL, MI, MS, and OH.