Recall of Sterile Drug Products by Cantrell Drug Company

PUBLISHED: Nov 21, 2016

Cantrell Drug Company is voluntarily recalling certain unexpired sterile drug products due to lack of sterility assurance. See the Press Release for a listing of affected products and lot numbers.

The recalled products were distributed nationwide to health care facilities from May 25 to October 31, 2016. Cantrell Drug Company will begin notifying its customers by email and phone and is arranging for the return of all recalled products. Consumers who have product subject to the recall should stop using it and contact the company.

To return medication or request assistance related to this recall, contact Cantrell Drug Company at 877-666-5222, Monday through Friday between 9 a.m. and 5 p.m. CST.

Healthcare professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA's MedWatch Safety Information and Adverse Event Reporting Program.

Read the MedWatch Safety Alert, including a link to the press release, at the link below.

Want to read the full alert and receive alert emails?

Browse Additional Alerts