Safety Alerts Saves Lives
Safety Alerts  
 
Home Privacy About Us Contact Us Change Preferences
SafetyAlerts
March 26, 2003

Tyco Healthcare Has Recalled Conray 43

(SafetyAlerts) - The Food and Drug Administration (FDA) has released the following information.


PRODUCT
Conray 43 (Iothalamate meglumine Injection USP 43%), 202 mg/mL Organically Bound Iodine, 100mL bottle, Rx only, For Intravascular Use, Sterile Solution, Mallinckrodt Inc., St Louis, MO. NDC 0019-3183-07. Recall # D-176-3.

CODE
Lot number B371D.

RECALLING FIRM/MANUFACTURER
Tyco Healthcare, Raleigh, NC, by telephone on June 25, 2001. Firm initiated recall is ongoing.

REASON
Misbranding; product has no immediate bottle label.

VOLUME OF PRODUCT IN COMMERCE
696 cases (12 units per case).

DISTRIBUTION
Nationwide.

 

 
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?

Sign-up for SafetyAlerts by Email -
The free internet newsletter that could
some day literally save your life - or
the life of someone you know.

 

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.