FDAFDA · Food and drugs·Recall number D-832-2013
Methotrexate Injection, USP, Preservative-Free, 1 g/40 mL (25 mg/mL), 40 mL Single Dose Vial, Rx only, Manufactured for: Sandoz Inc., Princeton, NJ 08540; Manufactured by: EBEWE Pharma Ges.m.b.H. Nfg.KG, A-4866 Unterach, AUSTRIA, NDC 66758-041-01.
Published August 14, 2013 · Recall initiated: May 20, 2013
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
Presence of Particulate Matter: Found during examination of retention samples.
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- Sandoz Incorporated
- Distributor
- Nationwide
- Lot
- Lot #: CL0996, Exp 12/13; and CJ4948, Exp 05/13
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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