D-0599-2017 Class II Terminated
FDA drug recall D-0599-2017 was initiated by Synergy Rx on February 10, 2017 and is designated Class II. Reason for recall: Lack of Assurance of Sterility: There are also CGMP Deviations. The recall status is terminated (terminated May 23, 2017). Affected quantity: N/A.
Recall Details
- Product Type
- Drugs
- Report Date
- March 22, 2017
- Initiation Date
- February 10, 2017
- Termination Date
- May 23, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- N/A
Product Description
CUSTOM LIGHTENING/BRIGHTENING CREAM, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
Reason for Recall
Lack of Assurance of Sterility: There are also CGMP Deviations.
Distribution Pattern
Nationwide within the United States
Code Information
All Lots