July 11, 2002
Fresenius Kabi Has Recalled Intralipid 20%
- The Food and Drug Administration (FDA) has released the following
Intralipid 20%, (20% I.V. Fat Emulsion), For Intravenous Use, 500 mL
bottles, Rx only, NDC 0336-0491-03. Recall # D-339-2.
Lot numbers MSI0205, NR66055, NR66056, NR66057, NR66058, NR66059, NR66062,
Fresenius Kabi, Clayton, NC, by letter dated May 16, 2002.
Firm initiated recall is ongoing.
Particulates: bottles may contain dark tan to brown particulate matter.
VOLUME OF PRODUCT IN COMMERCE