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Class II: temporary or reversible health riskTerminated

GM Manufacturing Noni Supplement Recall

Noni Supplement, Capsules

GM Manufacturing Inc. · Gardena, CA

Risk level
Class II
Reported by FDA
Aug 6, 2014
Recall ID
F-2267-2014
Check your lot numberHow we source this data

Summary

GM Manufacturing recalled Noni Supplement starting Jul 3, 2014. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-2267-2014 on Aug 6, 2014. Reason: GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements. Status: Terminated.

Why it was recalled

GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.

Product description

Noni Supplement, Capsules

Lot numbers, UPCs & expiration codes

9/23/13 > 9/30/13

Where it was sold

CA

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-2267-2014
Classification
Class II
Status
Terminated
Recall initiated
Jul 3, 2014
FDA report date
Aug 6, 2014
Quantity
200,100 units
Recall type
Voluntary: Firm initiated
Recalling firm
GM Manufacturing Inc.

Original FDA data

Every field from FDA enforcement report F-2267-2014, exactly as published.

Show all FDA fields
City
Gardena
State
CA
Status
Terminated
Country
United States
Event ID
68717
Address
1500 W 135th St
Code information
9/23/13 > 9/30/13
Postal code
90249-2230
Report date
Aug 6, 2014
Product type
Food
Recall number
F-2267-2014
Classification
Class II
Recalling firm
GM Manufacturing Inc.
Product quantity
200,100 units
Termination date
Sep 16, 2014
Reason for recall
GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Noni Supplement, Capsules
Distribution pattern
CA
Recall initiation date
Jul 3, 2014
Initial firm notification
Letter
Center classification date
Jul 31, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-2267-2014, published Aug 6, 2014. View the source record (openFDA) · FDA enforcement reports

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

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