Testosterone/Finasteride/Anastrozole 120 mg/10 mg/4 mg recall: Sterility Concern
Testosterone/Finasteride/Anastrozole 120 mg/10 mg/4 mg pellet Amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas…
Why was Testosterone/Finasteride/Anastrozole 120 mg/10 mg/4 mg recalled?
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot#: 20180111@104, BUD 07/10/2018.
- Product
- Testosterone/Finasteride/Anastrozole 120 mg/10 mg/4 mg pellet Amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas…
- Recalling firm
- Partell Specialty Pharmacy
- Quantity
- one vial
- Distribution
- NV only
- Recall date
- April 25, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)