Dietary Supplement labeled and recall: Labeling Error
Dietary Supplement labeled and packaged under the following: LIVERAID, 200 Count Softgels; LIVER AID, 200 Count Softgels; MAX Brand LIVER STRONG 200…
Why was Dietary Supplement labeled and recalled?
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot # LS122 UPC: 6 65176 82031 1, 6 65176 02434 4, and 0 65176 06068
- Product
- Dietary Supplement labeled and packaged under the following: LIVERAID, 200 Count Softgels; LIVER AID, 200 Count Softgels; MAX Brand LIVER STRONG 200…
- Recalling firm
- Healthmaxx Global Inc.
- Quantity
- 5775 bottles
- Distribution
- CA, MD, and NY
- Recall date
- October 2, 2013
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (food)