D3 Vitamin Liquid, 50 mL, OTC Non-Sterile. Dietary supplement.

Pharmatech LLC recalled D3 Vitamin Liquid, 50 mL, OTC Non-Sterile. in a Class II action, the FDA tier for products that may cause temporary or medically reversible health effects on Aug 8, 2016.

The FDA-published reason for this recall is: "Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia."

The product reached multiple states, recorded by the FDA as "FL, MI, MS, and OH." A multi-state footprint means the same lot can surface in households far from the producer. The recalling firm is based in Davie, FL. The recall covers 229,464 bottles of product. The FDA has Terminated this recall (first reported Nov 2, 2016), its final lifecycle state, indicating the agency considers the corrective action resolved. The historical record remains useful for tracking a brand's recall pattern over time.