Saint Paul, MN, United States
Hill-Rom Manufacturing, Inc. recalls
1 recall recorded since 2018, most recently on 12 November 2020. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 12 November 2020
- Terminated
- 10 November 2022
- Reason
- Under certain conditions, there is a risk for fire.
- 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.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0484-2021
- 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.
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.