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Class I: serious health riskTerminated

Nutra Manufacturing Gnc Recall

GNC, Womens Ultra Mega, Dietary Supplement, 180 Caplets,

Nutra Manufacturing · Greenville, SC

Risk level
Class I
Reported by FDA
Dec 14, 2016
Recall ID
F-0626-2017
Check your lot numberHow we source this data

Summary

Nutra Manufacturing recalled Gnc starting Nov 10, 2016. The FDA classified it as Class I (serious health risk) and published enforcement report F-0626-2017 on Dec 14, 2016. Reason: Undeclared Allergen: Milk. Status: Terminated.

Why it was recalled

Undeclared Allergen: Milk.

Product description

GNC, Womens Ultra Mega, Dietary Supplement, 180 Caplets,

Lot numbers, UPCs & expiration codes

GNC number: 202422, Nutra Manufacturing Lot Number: 3044FQ2024.

Where it was sold

PA

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0626-2017
Classification
Class I
Status
Terminated
Recall initiated
Nov 10, 2016
FDA report date
Dec 14, 2016
Quantity
12,534 bottles/180 caplets per bottle.
Recall type
Voluntary: Firm initiated
Recalling firm
Nutra Manufacturing

Original FDA data

Every field from FDA enforcement report F-0626-2017, exactly as published.

Show all FDA fields
City
Greenville
State
SC
Status
Terminated
Country
United States
Event ID
75738
Address
1050 Woodruff Rd
Code information
GNC number: 202422, Nutra Manufacturing Lot Number: 3044FQ2024.
Postal code
29607-4120
Report date
Dec 14, 2016
Product type
Food
Recall number
F-0626-2017
Classification
Class I
Recalling firm
Nutra Manufacturing
Product quantity
12,534 bottles/180 caplets per bottle.
Termination date
Jul 27, 2017
Reason for recall
Undeclared Allergen: Milk.
Voluntary / mandated
Voluntary: Firm initiated
Product description
GNC, Womens Ultra Mega, Dietary Supplement, 180 Caplets,
Distribution pattern
PA
Recall initiation date
Nov 10, 2016
Initial firm notification
E-Mail
Center classification date
Dec 7, 2016

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0626-2017, published Dec 14, 2016. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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