Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy recalls Heparin 20,000 U/Lidocaine 2% 10 mL/Sodium Bicarbonate 8.4% 10 mL/Sterile Water 5 mL, 27 mL Syringe, Anderson Compoundin
Recalled April 24, 2019 · FDA recall D-1156-2019 · Anderson Compounding Pharmacy, Inc.
Hazard
Lack of sterility assurance. · FDA Class II
Units
2 syringes
Sold at
Nationwide
Description
Lack of sterility assurance.
Product
Heparin 20,000 U/Lidocaine 2% 10 mL/Sodium Bicarbonate 8.4% 10 mL/Sterile Water 5 mL, 27 mL Syringe, 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 →