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FDAFDA · Food and drugs·Recall number D-0406-2022

Methotrexate, USP, Sterile Solution for Injection (PF), 125 mg/5mL (2mg/mL), 5 mL per syringe, Edge Pharma, LLC, 856 Hercules Dr, Colchester, VT 05446, NDC 05446-1505-05

Published February 2, 2022 · Recall initiated: December 6, 2021

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Lack of Assurance of Sterility

What to do

Voluntary: Firm initiated · Press Release

Recall details

Manufacturer
Edge Pharma, LLC
Distributor
nationwide
Lot
09-2021-10@2 12/23/2021, 10-2021-21@2 02/01/2022 & 11-2021-09@5 02/21/2022
Risk classification
Class II
Area (FDA)
drug
Country
United States

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