Duy Drugs Inc.: Food Recall in 2017 - (Recall #: F-3355-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Viva ben Femenine Supplement, Dietary Supplement 30 Softgels

Product Classification:

Class II

Date Initiated: July 21, 2017

Date Posted: August 16, 2017

Recall Number: F-3355-2017

Event ID: 77715

Reason for Recall:

Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.

Status: Terminated

Product Quantity: 1800 bottles

Code Information:

Lot No. 0117221

Distribution Pattern:

Domestic distribution only.

Voluntary or Mandated:

Voluntary: Firm initiated