Skip to content

FDA Recall Alert: Baxter Permanently Removes Life2000 Ventilation System

This recall involves removing certain devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it. Stop using Life2000 ventilators. Patients should reach out to their healthcare provider to discuss replacement options. Do not leave ventilators unattended in public or unsecured areas. For all healthcare-related customers (healthcare facilities, DME suppliers, and distributors): Locate and discontinue use of all Life2000 ventilators and compressors within the facility. Do not leave Life2000 Ventilation System unattended in public or unsecured areas. Maintaining physical possession and control of the ventilator reduces the likelihood of an unauthorized person gaining access to the device. If you suspect that a device has been exposed to unauthorized personnel, contact Baxter Acute Care Customer Service team. The team can help verify whether the device settings are correct and if the device is performing as expected. The team can be reached by email at HRC_ACCS_Web@baxter.com, or by phone at 800-426-4224, option 2, then option 1. Forward this communication to any departments within the institution who use the affected product.

Read more here.