PlainRecalls
FDA Drug Critical Class I Terminated

Levoleucovorin Injection, 250 mg/25 mL, (10 mg/mL), 25 mL Single-Use Vial, Rx only, Manufactured for: Mylan Institutional LLC, Rockford, IL 61103 U.S.A., Made in India. NDC: 67457-601-30

Reported: March 20, 2019 Initiated: February 1, 2019 #D-1059-2019

Product Description

Levoleucovorin Injection, 250 mg/25 mL, (10 mg/mL), 25 mL Single-Use Vial, Rx only, Manufactured for: Mylan Institutional LLC, Rockford, IL 61103 U.S.A., Made in India. NDC: 67457-601-30

Reason for Recall

Presence of Particulate Matter: particulate matter identified as copper salts

Details

Recalling Firm
Mylan Institutional Inc
Units Affected
11,964 cartons of 30 vials
Distribution
Nationwide in the United States
Location
Rockford, IL

Frequently Asked Questions

What product was recalled?
Levoleucovorin Injection, 250 mg/25 mL, (10 mg/mL), 25 mL Single-Use Vial, Rx only, Manufactured for: Mylan Institutional LLC, Rockford, IL 61103 U.S.A., Made in India. NDC: 67457-601-30. Recalled by Mylan Institutional Inc. Units affected: 11,964 cartons of 30 vials.
Why was this product recalled?
Presence of Particulate Matter: particulate matter identified as copper salts
Which agency issued this recall?
This recall was issued by the FDA Drug on March 20, 2019. Severity: Critical. Recall number: D-1059-2019.