Trilogy Evo O2 and LifeVent EVO2, Model Numbers DS2100X11B, IN2100X15B, IN2100X19, FX2100X15B, LA2100X15B, IA2100X15B, FP2100X10, FR2100X14B, ND2100X15B, IT2100X21B, ES2100X15B, DE2100X13B, EU2100X15B, EU2100X19, EE2100X15B, and SP2100X26B
Recall
- Recall Number
- Z-1650-2023
- Event Number
- 92048
- Firm
- Philips Respironics, Inc.
- FEI Number
- 2518422
- Product Code
- CBK
- Status
- Open, Classified
- Root Cause
- Under Investigation by firm
- Initiated
- May 1, 2023
- Posted
- June 2, 2023
- Address
- 1001 Murry Ridge Ln, Murrysville, PA, 15668-8517
Description
Trilogy Evo O2 and LifeVent EVO2, Model Numbers DS2100X11B, IN2100X15B, IN2100X19, FX2100X15B, LA2100X15B, IA2100X15B, FP2100X10, FR2100X14B, ND2100X15B, IT2100X21B, ES2100X15B, DE2100X13B, EU2100X15B, EU2100X19, EE2100X15B, and SP2100X26B
Environmental debris may accumulate on the internal machine flow sensor causing partial occlusion which may impact accurate delivery of pressure, volume, or flow. A malfunction caused by this issue can result in patient harm up to hypoxemia if not addressed by the care provider.
An URGENT Medical Device Correction notification letter was sent to customers on 5/1/23. Please take the actions below in order to prevent risk for your patients. Actions that must be taken by the user in order to prevent risks for patients. To help prevent accumulation of debris on the machine flow sensor: Use the Philips approved particulate filter which prevents a significant majority of airborne aerosols and particulate from entering the device. This filter must be replaced between patients and monthly as indicated in the Instructions for Use. Using this filter was previously optional. This is now required. Use the air inlet filter as indicated in the Instructions for Use. Installation of the particulate filter will not require a change to therapy settings. To help detect change in therapy: Set appropriate alarms based on ventilation mode, such as Low Tidal Volume, Low Minute Ventilation, Low Inspiratory Pressure, and High Inspiratory Pressure. Check Proximal Pressure and External Flow Sensor Failed alarms can also alert the user to this issue. These are non settable alarms. The device will issue a low priority Inlet Filter(s) Blocked alarm if therapy is reduced due to filter occlusion. The device will continue to function if this occurs, but the user must be aware to rinse the air inlet filter and replace the particulate filter if this occurs. Observe instructions for any alarm, especially Ventilator Service Required or Ventilator Inoperative. If the situation cannot be resolved, use alternative ventilation equipment. Ensure ventilator dependent patients have access to alternative ventilation equipment, such as a back up ventilator or manual resuscitator. Distribute this notice to all employees in your organization that need to be aware. Train device users within your network to use the air inlet and particulate filters on all patients. Send this notice to any organization an impacted device was sold or distributed to. If you need any further informatio
US Nationwide. Global Distribution.
21,520 devices