PlainRecalls
FDA Drug Moderate Class II Terminated

Clonidine Hydrochloride Tablets, USP, 0.1 mg, 100-count bottle, Rx only, MFG: Teva/Actavis, NDC 00228-2127-10

Reported: June 15, 2022 Initiated: April 13, 2022 #D-1066-2022

Product Description

Clonidine Hydrochloride Tablets, USP, 0.1 mg, 100-count bottle, Rx only, MFG: Teva/Actavis, NDC 00228-2127-10

Reason for Recall

cGMP deviations: Temperature abuse

Details

Units Affected
63 bottles/100 count
Distribution
USA nationwide.
Location
Richmond, VA

Frequently Asked Questions

What product was recalled?
Clonidine Hydrochloride Tablets, USP, 0.1 mg, 100-count bottle, Rx only, MFG: Teva/Actavis, NDC 00228-2127-10. Recalled by Mckesson Medical-Surgical Inc. Corporate Office. Units affected: 63 bottles/100 count.
Why was this product recalled?
cGMP deviations: Temperature abuse
Which agency issued this recall?
This recall was issued by the FDA Drug on June 15, 2022. Severity: Moderate. Recall number: D-1066-2022.