Edge Pharma, LLC recalls Phenylephrine HCl, Sterile Solution for Injection, (PF), 800 mcg/10mL (80 mcg/mL), Single Use Syringe for IV Injection,
Recalled February 2, 2022 · FDA recall D-0417-2022 · Edge Pharma
Hazard
Lack of Assurance of Sterility · FDA Class II
Units
5335 syringes
Sold at
nationwide
Description
Lack of Assurance of Sterility
Product
Phenylephrine HCl, Sterile Solution for Injection, (PF), 800 mcg/10mL (80 mcg/mL), Single Use Syringe for IV Injection, Edge Pharma, LLC 856 Hercules Dr., Colchester, VT 05446, NDC 05446-1652-01
Manufacturer(s)
Edge Pharma, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →