D-0654-2018 Class II Terminated
FDA drug recall D-0654-2018 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). Affected quantity: one vial.
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
- one vial
Product Description
Testosterone/Finasteride/Anastrozole 120 mg/10 mg/4 mg pellet 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#: 20180111@104, BUD 07/10/2018.