Sun Pharmaceutical Industries, Inc. recalls Vecuronium Bromide for Injection 20 mg* *1mg/mL when reconstituted to 20 mL Lyophilized, 10 x 20 mg vials, Rx Only, Manu
Recalled January 16, 2019 · FDA recall D-0373-2019 · Sun Pharmaceutical Industries
Hazard
Presence of Particulate Matter: Foreign matter identified as glass detected in Vecuronium Bromide for Injection. · FDA Class I
Units
1,384 cartons, 13,840 vials
Sold at
Nationwide in the USA
Description
Presence of Particulate Matter: Foreign matter identified as glass detected in Vecuronium Bromide for Injection.
Product
Vecuronium Bromide for Injection 20 mg* *1mg/mL when reconstituted to 20 mL Lyophilized, 10 x 20 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: 47335-932-40 [vial] 47335-932-44 [carton]
Manufacturer(s)
Sun Pharmaceutical Industries, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →