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September 29, 2003

Organon Has Recalled Zemuron Injection

(SafetyAlerts) - The FDA has released the following information.

Zemuron Injection, (rocuronium bromide) 10 mg/mL, For IV use only, professional sample of 6X5mL vials, 5mL and 10mL multiple dose vials. Recall # D-310-3.

Packaged Lot Numbers: 2442902450, exp. July 2004; 2453002450, exp. July 2004; 2463102450, exp. July 2004; 0583102450, exp. July 2004; 0593302450, exp. July 2004; 2483702450, exp. August 2004; 2493702450, exp. August 2004; 0023702450, exp. August 2004; 2513802450, exp. August 2004; 2623802450, exp. August 2004; 0634002450, exp. August 2004; 0644002450, exp. August 2004; Packaged Lot Numbers: 1483402450, exp. August 2004; 1493502450 exp. August 2004; 1503602450, exp. August 2004. The packaged lot number has an additional three digit packaging before the manufactured lot number.

Organon, Inc., West Orange, NJ, by letters on July 1, 2003. FDA initiated recall is ongoing.

Vials may contain metal particles.

1,582,420 vials.

Nationwide and Canada.

Selected Recent Recalls

Health Professional:

Did you know?
During 2000 there were over
1050 products recalled in the United
States for safety reasons!

How many did you hear about?

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The information contained herein has been obtained from sources that the Company believes to be reliable, however, the Company has not independently verified or confirmed the information and the recipient acknowledges that no representations or warranties are being made in connection with the use of the information.