On March 26, 2011 Greenstone LLC announced a voluntary nationwide recall of Citalopram and Finasteride medications due to the possibility that incorrect labels have been placed on the bottles by a third-party manufacturer.
If you or someone close to you has given birth to a child with a birth defect after taking improperly labeled Citalopram or Finasteride, you should contact our lawyers immediately for a free confidential case evaluation. You may be entitled to compensation for your injuries and we can help.
Greenstone LLC announced a nationwide recall of Citalopram 10mg Tablets (100-count bottle) with the lot number FI0510058-A after a possible labeling error was noticed. Bottles which had been labeled Citalopram Lot # FI0510058-A may contain Finasteride, an active ingredient that may cause potential harm to anyone who is unaware they are taking it.
The Greenstone LLC recall includes the following medications:
- Citalopram 10mg Tablets (100-count bottle) Lot # FI0510058-A
- Finasteride 5mg Tablets (90-count bottle) Lot # FI0510058-A
For more information on the recall, please visit the FDA’s website.
Finasteride is used for the treatment of benign prostatic hyperplasia. However, recent studies suggest there may be a link between the use of Finasteride and congenital birth defects. Women who unknowingly take Finasteride while pregnant may increase the risk of their child developing severe, life-threatening birth defects.
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If you or someone close to you has given birth to a child with a birth defect after taking improperly labeled Citalopram or Finasteride, you should contact our lawyers immediately by clicking the link below or calling toll free (949) 557-5800. You may be entitled to compensation for your injuries and we can help.