Recalls / Class II
Class IID-1004-2016
Product
PHENYLEPHERINE 0.5%, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
- Affected lot / code info
- Lot #: 01282016:60@3, Exp.04/28/2016; Lot #: 02242016: 90@20, Exp.05/24/2016; Lot #: 02222016:06@67, Exp. 05/24/2016; Lot #: 03082016:81@21, Exp.06/06/2016; Lot #: 03162016: 62@1, Exp. 06/14/2016.
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-1004-2016. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.