FDAFDA · Food and drugs·Recall number D-068-2013
Arranon (nelarabine) Injection 5mg/mL, 50mL Vials, Rx only, For I.V. Infusion only, GlaxoSmith Kline, Research Triangle Park, NC 27709. Made in England, NDC 0007-4401-06
Published December 5, 2012 · Recall initiated: October 8, 2012
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
Impurities/Degradation Products: Potential for drug related impurities to exceed the specification limits.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- GlaxoSmithKline, LLC.
- Distributor
- Nationwide
- Lot
- Lot # C536707 Exp 02/14, C538830 Exp.02/14, C533169 Exp. 02/14
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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