FDA Drug recall D-0130-2017
Estradiol 3 mg Pellet, Compounded by: Wells Pharmacy Network
- FDA Drug
- Class III
- terminated
- Published 2016-11-16
On 2016-11-16 the FDA classified a Class III recall of Estradiol 3 mg Pellet, Compounded by: Wells Pharmacy Network by Wells Pharmacy Network, citing superpotent and Subpotent drugs.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0130-2017 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2016-09-19 |
| Published | 2016-11-16 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Wells Pharmacy Network |
| Distribution | n/a |
Product
Estradiol 3 mg Pellet, Compounded by: Wells Pharmacy Network
Reason
Superpotent and Subpotent drugs
Identifiers
| code_info | Lot Number 08082016@1, BUD: 02/04/2017 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Other recalls by Wells Pharmacy Network
- Nicotinamide Adenine Dinucleotide (NADH) - Lyophilized (P.F.) 100 mg Injectable, Compounded by Wells Pharmacy, Ocala, FL
FDA Drug · Class II · 2017-01-11 · Wells Pharmacy Network - Forskolin/PAPAV/PHEN/PGE1, 100 mcg/30 mcg/3 mcg/60 mcg/mL, 5 mL vial, Injectable, Compounded by Wells Pharmacy, Ocala, FL
FDA Drug · Class II · 2017-01-11 · Wells Pharmacy Network - Chorionic Gonadotropin Lyophilized, 20,000 unit Injectable Kit, Compounded by Wells Pharmacy, Ocala, FL
FDA Drug · Class II · 2017-01-11 · Wells Pharmacy Network - TitanMax-MIC/12/CA/CH/L/D Injectable 25 mg/50 mg/50/0.5 mg/50 mg/25 mcg/25 mg/25 mg/mL, 30 mL vial, Compounded by Wells Pharmacy, Ocala, FL
FDA Drug · Class II · 2017-01-11 · Wells Pharmacy Network - Methylcobalamin Injectable (Dr. Hall Kit) - 1,000 mcg/mL, 30 mL vial Kit, Compounded by Wells Pharmacy, Ocala, FL
FDA Drug · Class II · 2017-01-11 · Wells Pharmacy Network
All Wells Pharmacy Network recalls
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0130-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.