Test Cypionate 200mg/anastrozole 0.5mg/dutasteride recall: Sterility Concern
TEST CYPIONATE 200MG/ANASTROZOLE 0.5MG/DUTASTERIDE 1.5MG/ML IN OIL INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25…
Why was Test Cypionate 200mg/anastrozole 0.5mg/dutasteride recalled?
Lack of assurance of sterility
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: T1007012021:96 BUD: 12/28/2021; T1008192021:04 BUD: 02/15/2022
- Product
- TEST CYPIONATE 200MG/ANASTROZOLE 0.5MG/DUTASTERIDE 1.5MG/ML IN OIL INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25…
- Recalling firm
- Vita Pharmacy, LLC dba Talon Compounding Pharmacy
- Quantity
- 4 vials
- Distribution
- United States including Washington, D.C. and Puerto Rico
- Recall date
- November 17, 2021
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)