Edge Pharma, LLC recalls Lidocaine HCl/Epinephrine, Sterile Buffered Solution for Injection (PF) 1% / 1:100,000, 3 mL per syringe, Edge Pharma, L
Recalled February 2, 2022 · FDA recall D-0396-2022 · Edge Pharma
Hazard
Lack of Assurance of Sterility · FDA Class II
Units
8140 syringes
Sold at
nationwide
Description
Lack of Assurance of Sterility
Product
Lidocaine HCl/Epinephrine, Sterile Buffered Solution for Injection (PF) 1% / 1:100,000, 3 mL per syringe, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT 05446, (802) 992-1178, NDC 05446-1268-01
Manufacturer(s)
Edge Pharma, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →