D-1282-2015 Class II Terminated
FDA drug recall D-1282-2015 was initiated by Mutual Pharmaceutical Company, Inc. on July 9, 2015 and is designated Class II. Reason for recall: cGMP Deviations; Clonidine hydrochloride drug substance used in the manufacturing of this product, was dispensed in unauthorized rooms by the drug substance manufacturer The recall status is terminated (terminated October 13, 2016). Affected quantity: 20,892 bottles.
Recall Details
- Product Type
- Drugs
- Report Date
- August 5, 2015
- Initiation Date
- July 9, 2015
- Termination Date
- October 13, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 20,892 bottles
Product Description
Clonidine Hydrochloride Tablets, USP, 0.3 mg, 100 count HDPE bottles, Rx only, Mutual Pharmaceutical, Philadelphia, PA, NDC 53489-217-01
Reason for Recall
cGMP Deviations; Clonidine hydrochloride drug substance used in the manufacturing of this product, was dispensed in unauthorized rooms by the drug substance manufacturer
Distribution Pattern
Nartionwide
Code Information
Lot #: 6676701 and 6676801, exp 1/17