Wellness Pharmacy, Inc. Issues Nationwide Voluntary Recall of Certain Sterile Products

Recall issued due to lab results indicating microbial contamination

/ Author:  / Reviewed by: Joseph V. Madia, MD Beth Bolt, RPh

This recall was initiated after Wellness Pharmacy was notified that in a recent inspection of Front Range Labs, FDA investigators observed methods used by Front Range Labs to assess sterility and other qualities (e.g., strength and stability) may have resulted in Wellness Pharmacy receiving inaccurate sterility test results on these lots.

FDA has concerns that test results obtained from Front Range Labs may not be reliable.

For a list of medications that are being voluntarily recalled, click here.

If there is microbial contamination in medications intended to be sterile, patients are at risk of serious infections which may be life threatening. To date Wellness Pharmacy has not received any reports of adverse events related to this recall.

Recalled medications were distributed to individual patients and to physician offices nationwide. These liquid medications are in either clear or amber sterile vials ranging in size from 1ml to 50ml. The medications can be identified by the label on each vial, which will have the name of the drug, strength or concentration, lot number, use by date, and vial size.

Wellness Pharmacy is notifying its customers by telephone and regular mail of this recall. Patients and physicians should immediately discontinue use of these lots of medications, and return the recalled unexpired medications to Wellness Pharmacy.

To return medication or request assistance related to this recall, patients and physicians should contact Wellness Pharmacy at 205-879-6551 or 800-227-2627, Monday through Friday, between 9 am and 4 pm CDT.

Patients should contact their physician or health care provider if they have experienced any problems that may be related to taking these medications.

Adverse reactions experienced with the use of these medications may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

Review Date: 
August 27, 2013
Last Updated:
August 27, 2013