GNC, Womens Ultra Mega, Dietary Supplement, 180 Caplets
Recalling firm: Nutra Manufacturing
Why it was recalled
Undeclared Allergen: Milk.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jul 27, 2017.
Check your package
Compare the exact product and package details with the label you have.
ProductGNC, Womens Ultra Mega, Dietary Supplement, 180 Caplets,
FDA code information
GNC number: 202422, Nutra Manufacturing Lot Number: 3044FQ2024.
Match the product, package size, and code together. A missing match does not guarantee safety.
Full FDA record and distribution details
Original product description
GNC, Womens Ultra Mega, Dietary Supplement, 180 Caplets,
Original FDA recall reason
Undeclared Allergen: Milk.
Recall details
- Recall number
- F-0626-2017
- Event ID
- 75738
- FDA status
- Terminated
- Initiated
- Nov 10, 2016
- Reported
- Dec 14, 2016
- Classified
- Dec 7, 2016
- Terminated
- Jul 27, 2017
- Quantity
- 12,534 bottles/180 caplets per bottle.
- Location
- Greenville, SC, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
Where it was distributed
PA
FDA source record · F-0626-2017
Data updated September 16, 2026. View official FDA data ↗
Follow official FDA and manufacturer guidance.