Recall · openFDA Food Enforcement

GNC, Women s Ultra Mega, Dietary Supplement, 180 Caplets,: FDA Recall F-0626-2017

Agency action: Nov 10, 2016Record ID: F-0626-2017
View official source ↗

What happened

Original notice title

GNC, Women s Ultra Mega, Dietary Supplement, 180 Caplets,, recall F-0626-2017

From the archived source record

Undeclared Allergen: Milk.

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 I
Recall initiated by
Voluntary: Firm initiated
Report date
Dec 14, 2016
Termination date in the archive
Jul 27, 2017
Source checked
Jul 16, 2026
Record revision
978feb207b5c

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
GNC, Women s Ultra Mega, Dietary Supplement, 180 Caplets,
Company
Nutra Manufacturing
Lot / identifier
GNC number: 202422, Nutra Manufacturing Lot Number: 3044FQ2024.
Market / distribution
PA