Edge Pharma, LLC recalls Phenylephrine HCl/Lidocaine, Sterile Ophthalmic Solution for Injection, Preservative Free, 1.5%/1%, 0.8mL per syringe, S
Recalled February 2, 2022 · FDA recall D-0419-2022 · Edge Pharma
Hazard
Lack of Assurance of Sterility · FDA Class II
Units
2750 syringes
Sold at
nationwide
Description
Lack of Assurance of Sterility
Product
Phenylephrine HCl/Lidocaine, Sterile Ophthalmic Solution for Injection, Preservative Free, 1.5%/1%, 0.8mL per syringe, Single Use Syringe For Intraocular Injection, Edge Pharma LLC, 856 Hercules Dr, Colchester, VT 05446, NDC 05446-1118-01
Manufacturer(s)
Edge Pharma, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →