FDAJanuary 25, 2023device
Life2000 Ventilator , REF MS-01-0118, ventilatory support for the care of individuals
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
There is the potential for patient desaturation events to occur under certain scenarios when the Life2000 ventilation system is connected with an oxygen concentrator.
What to do
FDA enforcement status: Ongoing
Brands named
baxter healthcarebaxter
UPCs
00887761978089
Recall history
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- FDAGE Healthcare Omnipaque (iohexol) Injection, 300 mg/mL (64.7%), Rx Only, Distributed by: GE Healthcare Inc., Marlborough, MA 01752 USA, NDC 0407-1413-63.2026-03-24
- FDAGE Healthcare Omnipaque (iohexol) Injection, 350 mg/mL (64.7%), Rx Only, Distributed by: GE Healthcare Inc., Marlborough, MA 01752 USA, NDC 0407-1414-91.2026-03-24
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