October 10, 2002
Recall Update: Laurel Home Healthcare
Liquid Oxygen Recall Complete
The Food and Drug
Administration (FDA) released the following information.
Liquid Oxygen, USP, Refrigerated, transfilled into 46 liter Cryogenic Home
Vessels, Rx Only. Recall # D-002-3.
Serial numbers: 02182013, 01253095, 01190133, 01190112, 01190110, 02204388,
01180794, 01180787, 01180187, 01150090, 01150072.
Laurel Home Healthcare, Ann Arbor, MI, by telephone on September 20, 2002.
Firm initiated recall is ongoing.
Good Manufacturing Practice (GMP) deviations, including but not limited to,
lack of all batch records and use of an improperly calibrated oxygen
VOLUME OF PRODUCT IN COMMERCE