FDA recall record

Mylan Institutional Levoleucovorin Injection, 250 mg/25 mL, (10 mg/mL), 25 mL Single-Use recall — FDA D-1059-2019

Presence of Particulate Matter: particulate matter identified as copper salts

Class Iclassification
D-1059-2019official record ID
Mar 20, 2019report date

Recall record at a glance

Official recordD-1059-2019
CategoryDrug Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmMylan Institutional Inc.
Report dateMar 20, 2019
Recall initiation dateFeb 1, 2019
Quantity11,964 cartons of 30 vials
LocationRockford, IL, United States

Official 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

Why the product was recalled

Presence of Particulate Matter: particulate matter identified as copper salts

Distribution information

Nationwide in the United States

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.