MedicineWatch US
Class II Recall

Edge Pharma, LLC

Product
Phenol, Sterile Solution for Injection (PF), 6%, 5 mL per vial, Single Use Vial for Perineural Injection, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT 05446, NDC 05446-1476-05, packaged in vials.
Reason
Lack of Assurance of Sterility
Classification
Class II
Status
Terminated
Lot
09-2021-14@5 12/29/2021, 10/21/21 & 11-2021-04@2, 02/15/2022
Date
Disclaimer: This tool indexes published US FDA drug-enforcement recall records from all countries, limited to the latest five years. A company or product not appearing here is not proof that it is compliant, approved, safe, or free of FDA action.
Edge Pharma, LLC — Class II Recall | MedicineWatch US