PlainRecalls
FDA Drug Critical Class I Terminated

Vecuronium Bromide for Injection, For IV use only, 20 mg per vial, 10 x 10 mg Vials, lyophilized powder per carton, Rx Only, Mfr. By: Ben Venue Laboratories, Bedford, OH 44146: Mfg for: Bedford Labs, Bedford, OH 44146, NDC 55390-039-10.

Reported: October 3, 2012 Initiated: June 26, 2012 #D-1697-2012

Product Description

Vecuronium Bromide for Injection, For IV use only, 20 mg per vial, 10 x 10 mg Vials, lyophilized powder per carton, Rx Only, Mfr. By: Ben Venue Laboratories, Bedford, OH 44146: Mfg for: Bedford Labs, Bedford, OH 44146, NDC 55390-039-10.

Reason for Recall

Presence of Particulate Matter

Details

Units Affected
797 boxes/10/20 mg vials
Distribution
Nationwide
Location
Bedford, OH

Frequently Asked Questions

What product was recalled?
Vecuronium Bromide for Injection, For IV use only, 20 mg per vial, 10 x 10 mg Vials, lyophilized powder per carton, Rx Only, Mfr. By: Ben Venue Laboratories, Bedford, OH 44146: Mfg for: Bedford Labs, Bedford, OH 44146, NDC 55390-039-10.. Recalled by Ben Venue Laboratories Inc. Units affected: 797 boxes/10/20 mg vials.
Why was this product recalled?
Presence of Particulate Matter
Which agency issued this recall?
This recall was issued by the FDA Drug on October 3, 2012. Severity: Critical. Recall number: D-1697-2012.