Important Patient Announcement: Duloxetine (Cymbalta) Recall

Dear Patients,
The FDA has recently issued a voluntary recall of Duloxetine (Cymbalta) capsules manufactured by Rising Pharmaceuticals due to the presence of a potentially cancer-causing chemical. This recall affects more than 233,000 bottles and has been classified as a Class II risk, which means it could cause temporary or medically reversible adverse health effects.
What You Need to Do:

• Check Your Manufacturer: If you are currently taking Duloxetine (Cymbalta), please contact your pharmacy to determine if your prescription was manufactured by Rising Pharmaceuticals.

• Request a Replacement: If your medication is affected, ask your pharmacy to replace it with Duloxetine from a different manufacturer.

If You Wish to Stop Duloxetine:

• Do Not Stop Abruptly: Stopping Duloxetine suddenly can result in withdrawal symptoms or worsening of your condition.

• Schedule an Appointment: If you would like to discuss alternative treatment options or stopping Duloxetine, please schedule an appointment with your provider. We will work with you to develop a safe and effective plan tailored to your needs.

Your health and safety are our top priorities. If you have any questions or concerns, please don’t hesitate to reach out to our office.