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According to recent reports, Actavis Totowa, the makers of Digitek, have recalled all generic drugs manufactured at their New Jersey plant.
The recall comes in the aftermath of an inspection conducted at the plant in Little Falls by the FDA earlier this year.
The FDA reported the Actavis plant didn’t meet standards for good manufacturing practices.
As a result, Actavis has issued the voluntary recall of their products from pharmacies, hospitals and retailers.
In April, Actavis Totowa recalled their widely used Digitek tablets after research showed the medication contained twice the amount of the active ingredient meant to be contained in the tablets.
Some of the faulty tablets found were reportedly produced at the New Jersey plant now in question.
Since the recall of Digitek, there have been several reports of Side Effects in patients who were prescribed the drug.
The FDA supposedly issued a warning letter to Actavis in 2006 for their failure to provide safety reports at the New Jersey plant.
Among the drugs that have been recalled are Amidrine capsules, Cilostazol tablets 100mg and Naltrexone 50mg tablets.
(Source: UPI.com)
Have you been harmed by taking Digitek or another drug that has been recalled? If so, please contact us to speak with an experienced attorney who will enable you to receive the legal guidance and support you need and deserve in your case.