FDAFDA · Food and drugs·Recall number D-0625-2017
Kalbitor (ecallantide), 10mg/mL, packaged in 3 vials per Carton, Rx Only, Dynax Corp., Burlington, MA. NDC47783-101-01
Published April 12, 2017 · Recall initiated: March 17, 2017
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: Glass
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- KALBITOR
- Manufacturer
- Shire
- Distributor
- Nationwide and Kuwait
- Lot
- Lot #: A1500009, Exp. Jan 31, 2019
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.