Solodyn Recalled: Wrong Ingredients

Lots of Solodyn have been recalled by Medicis as they contain Azasan instead of Solodyn.

The recalled lots of Solodyn are:

B080037 (Exp: 12/09)

B080038 (Exp: 12/09)

Extended Release Tablets, 90 mg, 30-count bottles (NDC 99207-461-30)

Azasan is used in transplant patients to prevent organ rejection, and is also used to treat rheumatoid arthritis. Side effects of taking Azasan include decreased red and white blood cells, infection, bleeding, chills, nausea, vomiting and diarrhea, and may also instigate interactions with other drugs taken by patients.

Taking the incorrect medication may adversely affect patients.

Solodyn in the News

MAY-16-08: Medicis Announces Voluntary Recall of Solodyn® (minocycline HCL, USP) 90 Mg Tablets, Extended Release; Lot Numbers B080037 and B080038 Due to Product Mix-Up. [FDA: SOLODYN RECALL]

Legal Help

If you or a loved one has suffered damages due to Solodyn containing Azasan, please click the link below to send your complaint to a lawyer to evaluate your claim at no cost or obligation.