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Sun Pharmaceutical Industries, Inc. recalls Vecuronium Bromide for Injection 10 mg*, *1mg/mL when reconstituted to 10 mL Lyophilized, 10 x 10 mg vials, Rx only, Man

Recalled January 16, 2019 · FDA recall D-0372-2019 · Sun Pharmaceutical Industries

Hazard
Presence of Particulate Matter: Foreign matter identified as glass detected in Vecuronium Bromide for Injection. · FDA Class I
Units
12,534 cartons, 125,340 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 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]
Manufacturer(s)
Sun Pharmaceutical Industries, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Sun Pharmaceutical Industries, Inc. recalls Vecuronium Bromide for Injection 10 mg*, *1mg/mL when reconstituted to 10 mL Lyophilized, 10 x 10 mg vials, Rx only, Man | RecallWatchUSA