Recalls / Active ingredient / Clonidine Hydrochloride
Clonidine Hydrochloride
6 FDA drug recalls involving the active ingredient “Clonidine Hydrochloride”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2022-09-19 | Class III | Clonidine Hydrochloride Tablets, USP, 0.3 mg, 100-count bottle, Rx Only, Manufactured by: UNICHEM LABORATORIES | UNICHEM PHARMACEUTICALS USA INC |
| 2022-04-13 | Class II | Duraclon (clonidine HCl injection, USP), 1000 mcg/10 mL (100 mcg/mL), 10 mL single-dose vial, Rx only, MFG: My | Mckesson Medical-Surgical Inc. Corporate Office |
| 2020-05-26 | Class III | Clonidine Hydrochloride Tablets, USP 0.1 mg 100-count bottles, Rx only, Manufactured by: Unichem Laboratories | UNICHEM PHARMACEUTICALS USA INC |
| 2020-01-29 | Class III | Clonidine Hydrochloride Tablets, USP 0.1mg, Rx Only, 100-count bottle, Manufactured by: Unichem Laboratories L | UNICHEM PHARMACEUTICALS USA INC |
| 2019-03-29 | Class III | Clonidine HCL Injection, 1000 mcg/10mL (100 mcg/mL), 10 ML Single Dose Vial, Rx only, Manufactured for: X-Gen | X-Gen Pharmaceuticals Inc. |
| 2014-07-17 | Class III | Clonidine HCl Injection, 1000 mcg/10 mL (100 mcg/mL),10 mL Single Dose Vial, Rx only, Manufactured for: X-Gen | X-Gen Pharmaceuticals Inc. |