D-1333-2016 Class II Terminated
FDA drug recall D-1333-2016 was initiated by Pharmakon Pharmaceuticals, Inc. on April 20, 2016 and is designated Class II. Reason for recall: Lack of Assurance of Sterility The recall status is terminated (terminated January 11, 2018). Affected quantity: 1925.
Recall Details
- Product Type
- Drugs
- Report Date
- July 20, 2016
- Initiation Date
- April 20, 2016
- Termination Date
- January 11, 2018
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1925
Product Description
Rocuronium 10 mg/mL, 5 mL syringe, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0955-70
Reason for Recall
Lack of Assurance of Sterility
Distribution Pattern
Nationwide VA/DOD: CA, KY, MD, NC, OK, TX, VA
Code Information
All Sterile Compounded Products within Expiry