US Food Recall Atlas

A single recall record, as the agency published it.

Recall mapAll recalls → F-0268-2017

D-Vita Drops, 50 mL, OTC Non-Sterile. Dietary supplement. Pharmatech LLC · reported 2016-11-02

Terminated This recall has been closed out by the agency.

Reason for recall
Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Classification
Class II
Recall initiated
2016-08-08
Reported by the agency
2016-11-02
Closed out (terminated)
2024-09-23
Recalling firm
Pharmatech LLC
Davie, FL
United States

This is the firm that issued the recall — commonly a distributor or processor. It is not the origin of contamination.

Distribution (the agency's own words)
FL, MI, MS, and OH.
States we parsed from that text
FL MI MS OH

The agency named these states. Parse method explicit_state_list, confidence high.

Food category
Dietary supplementsderived

Assigned by a reviewed keyword rulebook over the product description, not by the agency.

Recall type
Voluntary: Firm initiated
Recall number
F-0268-2017

This page reproduces a record published by the US Food and Drug Administration. It is not real-time: recalls typically appear in FDA's Enforcement Report weeks after they begin — a median of 40 days, see publication lag. For current food safety information consult FDA and USDA FSIS directly.