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SafetyAlerts
October 1, 2003

Recall Update: Air Liquide America Oxygen Recall is Complete

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

PRODUCT
Oxygen, USP, compressed, cylinders (125 and 281-cubic ft), RX only. Recall # D-334-3.

CODE
Lot number 184SPO3018B-Exp date 07/03/08.

RECALLING FIRM/MANUFACTURER
Air Liquide America LP, Houston, TX, by letter dated July 17, 2003. Firm initiated recall is complete.

REASON
Good Manufacturing Practices deviation; failure to maintain cylinder fill and testing records.

VOLUME OF PRODUCT IN COMMERCE
36 cylinders.

DISTRIBUTION
WA.

 
Selected Recent Recalls


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During 2000 there were over
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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.