D-0668-2018 Class II Terminated

Recalled by Partell Specialty Pharmacy — Las Vegas, NV

FDA drug recall D-0668-2018 was initiated by Partell Specialty Pharmacy on March 22, 2018 and is designated Class II. Reason for recall: Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization. The recall status is terminated (terminated January 15, 2019).

Recall Details

Product Type
Drugs
Report Date
April 25, 2018
Initiation Date
March 22, 2018
Termination Date
January 15, 2019
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity

Product Description

Testosterone 55 mg pellet packaged in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800

Reason for Recall

Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.

Distribution Pattern

NV only

Code Information

Lot#: 20171024@53, BUD 04/22/2018; 20180219@91, BUD 08/18/2018.