Safety Alerts Saves Lives
Safety Alerts  
 
Home Privacy About Us Contact Us Change Preferences

SafetyAlerts
October 10, 2002

Recall Update: Laurel Home Healthcare Liquid Oxygen Recall Complete

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

PRODUCT
Liquid Oxygen, USP, Refrigerated, transfilled into 46 liter Cryogenic Home Vessels, Rx Only. Recall # D-002-3.

CODE
Serial numbers: 02182013, 01253095, 01190133, 01190112, 01190110, 02204388, 01180794, 01180787, 01180187, 01150090, 01150072.

RECALLING FIRM/MANUFACTURER
Laurel Home Healthcare, Ann Arbor, MI, by telephone on September 20, 2002. Firm initiated recall is ongoing.

REASON
Good Manufacturing Practice (GMP) deviations, including but not limited to, lack of all batch records and use of an improperly calibrated oxygen analyzer.

VOLUME OF PRODUCT IN COMMERCE
11 units.

DISTRIBUTION
MI.

 
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.