FDA Drug Recalls

Recalls / Class II

Class IID-1023-2016

Product

VITAMIN B COMPLEX # 1; packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121

Affected lot / code info
Lot #: 01120J67: 6@22, Exp. 04/12/2016; Lot #: 021820J6 : 52@39, Exp.04/18/2016; Lot #: 02262016: 89@3, Exp. 04/26/2016; Lot #: 03082016 : 76@46 06/06/2016;03022016:61@8, Exp. 06/08/2016; 032120 16:49@65, Exp.06/21/2016; 01152016:48@14, Exp. 04/19/2016; 03032016:74@52, Exp. 05/02/2016; 03242016:68@13, Exp. 06/27/2016; 04142016:00@50, Exp. 06/13/2016.

Why it was recalled

Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.

Recalling firm

Firm
Well Care Compounding Pharmacy
Notification channel
Press Release
Type
Voluntary: Firm initiated
Address
3430 E Tropicana Ave Ste 9, N/A, Las Vegas, Nevada 89121-7345

Distribution

Quantity
869 Units (Total All Products)
Distribution pattern
NV

Timeline

Recall initiated
2016-05-17
FDA classified
2016-06-09
Posted by FDA
2016-06-15
Terminated
2017-01-13
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1023-2016. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.