Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy recalls Lidocaine 1%/Dextrose 12.5% (PF) Injection, 10 mL Vial, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.
Recalled April 24, 2019 · FDA recall D-1188-2019 · Anderson Compounding Pharmacy, Inc.
Hazard
Lack of sterility assurance. · FDA Class II
Units
N/A
Sold at
Nationwide
Description
Lack of sterility assurance.
Product
Lidocaine 1%/Dextrose 12.5% (PF) Injection, 10 mL Vial, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.
Manufacturer(s)
Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →