Testosterone 60 mg/Anastrazole 4 mg Pellet, Compounded by: Wells Pharmacy Network
FDA Drug Recall #D-0128-2017 — Class II — September 19, 2016
Recall Summary
| Recall Number | D-0128-2017 |
| Classification | Class II — Moderate risk |
| Date Initiated | September 19, 2016 |
| Status | Terminated |
| Voluntary | Voluntary: Firm initiated |
Recalling Firm
| Firm | Wells Pharmacy Network, LLC |
| Location | Dyersburg, TN |
| Product Type | Drugs |
| Quantity | 358 pellets |
Product Description
Testosterone 60 mg/Anastrazole 4 mg Pellet, Compounded by: Wells Pharmacy Network
Reason for Recall
Superpotent and Subpotent drugs
Distribution Pattern
U.S.
Lot / Code Information
Lot Number 08012016@2, BUD 01/28/2017
Other Recalls from Wells Pharmacy Network, LLC
| Recall # | Classification | Product | Date |
|---|---|---|---|
| D-0126-2017 | Class II | Testosterone 200 mg/Anastrozole 9 mg Pellet, Co... | Sep 19, 2016 |
| D-0127-2017 | Class III | Testosterone Cholesterol ,100 mg Pellet, Compo... | Sep 19, 2016 |
| D-0129-2017 | Class III | Testosterone 12.5 mg Pellet, Compounded by: Wel... | Sep 19, 2016 |
| D-0131-2017 | Class II | Testosterone 200 mg/Anastrazole 20mg Pellet, Co... | Sep 19, 2016 |
| D-0132-2017 | Class III | Estradiol 12.5 mg Pellet, Compounded by: Wells... | Sep 19, 2016 |
Frequently Asked Questions
Stop taking the medication and contact your pharmacist or doctor immediately. For Class I recalls, this is urgent. For Class II or III recalls, consult your doctor before stopping — abruptly discontinuing certain medications (blood pressure drugs, antidepressants, diabetes medications) can be more harmful than continuing while arranging a replacement. Check whether the recall applies to your specific lot number and expiration date. Return the product to your pharmacy and report any adverse effects to FDA MedWatch at 1-800-FDA-1088.
Not necessarily. Many drug recalls are initiated because of quality system failures or test results that suggest a product might not meet specifications — even if no patients have reported harm. The FDA uses a precautionary approach: if there is reason to believe quality standards were not met, a recall is required regardless of whether adverse effects have been reported. Class I recalls typically involve a reasonable probability of harm; Class II recalls may cause temporary health issues; Class III recalls are for products unlikely to cause adverse health consequences but that still violate regulations.
Pharmacies typically receive recall notices directly from drug wholesalers and manufacturers within days of the recall being announced. Your pharmacist can look up whether any product in your prescription history matches a recalled lot number. For current recalls, the FDA publishes updates at FDA.gov/safety/recalls-market-withdrawals-safety-alerts and sends MedWatch email alerts for significant drug safety issues. You can sign up for MedWatch alerts at FDA.gov. Most major pharmacy chains also have their own recall notification systems that automatically alert pharmacists when a recalled product is in their inventory.
What Should You Do?
Stop using this medication if affected by this recall. Contact your pharmacist or prescribing doctor immediately for guidance. Do not flush medications — use a drug take-back program.