FDAFDA · Food and drugs·Recall number D-0372-2019
Vecuronium Bromide for Injection 10 mg*, *1mg/mL when reconstituted to 10 mL Lyophilized, 10 x 10 mg vials, Rx only, Manufactured by: Sun Pharmaceutical Industries Ltd. Halol-Baroda Highway Halol-389 350, Gujarat, India. Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512 NDC 47335-931-40 [vial] NDC 47335-931-44 [carton]
Published January 16, 2019 · Recall initiated: January 3, 2019
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: Foreign matter identified as glass detected in Vecuronium Bromide for Injection.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- VECURONIUM BROMIDE
- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Distributor
- Nationwide in the USA
- UPC
- 0347335932447
- Lot
- Lot #: JKS0443A, JKS0444A, JKS0477A, EXP 03/2019
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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