D-0905-2017 Class II Terminated
FDA drug recall D-0905-2017 was initiated by Safecor Health, LLC on July 7, 2016 and is designated Class II. Reason for recall: CGMP Deviations The recall status is terminated (terminated July 12, 2017). Affected quantity: 1,933 bottles.
Recall Details
- Product Type
- Drugs
- Report Date
- June 21, 2017
- Initiation Date
- July 7, 2016
- Termination Date
- July 12, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1,933 bottles
Product Description
Metronidazole 500mg Tablet, 50-count bottles, Rx only, Packaged By Safecor Health LLC Woburn, MA 01801, NDC 5011133402
Reason for Recall
CGMP Deviations
Distribution Pattern
MA and NY
Code Information
Lot # A25593, Exp. 02/22/2017