Life2000 Ventilation System, including Life2000 Ventilator and Life2000 Compressor, Model MS-01-0118 - Product Usage: use in home and institutional settings and is not intended for ambulance or air transport.
Reported: December 2, 2020 Initiated: November 12, 2020 #Z-0484-2021
Product Description
Life2000 Ventilation System, including Life2000 Ventilator and Life2000 Compressor, Model MS-01-0118 - Product Usage: use in home and institutional settings and is not intended for ambulance or air transport.
Reason for Recall
Under certain conditions, there is a risk for fire.
Details
- Recalling Firm
- Hill-Rom Manufacturing, Inc.
- Units Affected
- 67 devices
- Distribution
- US Nationwide distribution including in the states of AR, AZ, CA, DE, FL, IL, IN, KY, MN, NC, NM, NV, NY, OH, OK, TX, UT, VA, VT, WI.
- Location
- Saint Paul, MN
Frequently Asked Questions
What product was recalled? ▼
Life2000 Ventilation System, including Life2000 Ventilator and Life2000 Compressor, Model MS-01-0118 - Product Usage: use in home and institutional settings and is not intended for ambulance or air transport.. Recalled by Hill-Rom Manufacturing, Inc.. Units affected: 67 devices.
Why was this product recalled? ▼
Under certain conditions, there is a risk for fire.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 2, 2020. Severity: Moderate. Recall number: Z-0484-2021.
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