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SafetyAlerts
July 11, 2002

Fresenius Kabi Has Recalled Intralipid 20%

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

PRODUCT
Intralipid 20%, (20% I.V. Fat Emulsion), For Intravenous Use, 500 mL bottles, Rx only, NDC 0336-0491-03. Recall # D-339-2.

CODE
Lot numbers MSI0205, NR66055, NR66056, NR66057, NR66058, NR66059, NR66062, NR66063.

RECALLING FIRM/MANUFACTURER
Fresenius Kabi, Clayton, NC, by letter dated May 16, 2002.
Firm initiated recall is ongoing.

REASON
Particulates: bottles may contain dark tan to brown particulate matter.

VOLUME OF PRODUCT IN COMMERCE
25,200 units.

DISTRIBUTION
Nationwide.

 
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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.