Drug recall D-0553-2021
Product
Methotrexate Injection, USP 50 mg/2mL (25 mg/mL) 5 x 2mL Single-Dose Vials, Sterile, Rx Only, Distributed by Hospira, Inc. Lake Forest, IL 60045. NDC 61703-350-38.
Reason for recall
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots and codes
H074437AA
Recall details
- Recalling firm
- Cardinal Health Inc., Dublin, OH
- Quantity
- 341 vials
- Distribution
- FL, GA, SC
- Type
- Voluntary: Firm initiated
- Recall initiated
- March 15, 2021
- Terminated
- June 17, 2024
Related products
- Methotrexate – drug information
- NDC 61703-408 Methotrexate · Methotrexate Sodium 25 mg/mL · Hospira, Inc.
- NDC 61703-350 Methotrexate · Methotrexate Sodium 25 mg/mL · Hospira, Inc.