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Apotex Corp Recalls Birth Control Pill Over Defective Packaging

John Curiel1 year ago

In coordination with the FDA, Canadian pharmaceutical company Apotex Corp. has recalled four lots of Drospirenone and Ethinyl Estradiol Tablets, USP. Drospirenone and Ethinyl Estradiol is an estrogen/progesterone contraceptive.

Information About the Birth Control Recall

According to WAFB9, the drug may contain defective blisters and incorrect tablet placement, while the package may be missing some tablets altogether.

Women who try taking the affected birth control pills might accidentally take a placebo instead of an active tablet, or the appropriate tablet could be missing. Taking birth control pills the wrong way could  lead to unplanned pregnancy and other health complications.

Currently, there are no reports of unplanned pregnancy attributed to the affected pills.

FDA Urges Women to Consult Pharmacy and Healthcare Provider

The FDA urges women to return the affected pills to their local pharmacy and consult with their physician about possible alternatives.

The following lots are part of the recall:

  • 7DY008A
  • 7DY009A
  • 7DY010A
  • 7DY011A

The package contains 21 active yellow tablets and seven placebo tablets.

Contact an Experienced Dangerous Drug Attorney

If you or a loved one has been the victim of a dangerous pharmaceutical drug or medical device, you may be entitled to compensation. You deserve dynamic representation from a law firm with the resources necessary to take on the pharmaceutical companies. Thomas J. Henry has a track record of helping clients receive record-breaking verdicts, settlements, and judgments.

Our firm has offices in Corpus ChristiSan Antonio, Austin, and Houston, serving clients across Texas and nationwide. Call us today for a free case review — attorneys are available 24/7, nights and weekends.


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