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.
Check against the official notice below — it lists the full affected range.
Hill-Rom Manufacturing, Inc. is recalling 67 Life2000 Ventilation Systems, which include Life2000 Ventilators and Life2000 Compressors (Model MS-01-0118), used in home and institutional settings. The devices have been distributed nationwide across multiple states including California, Florida, New York, Texas, and others. Under certain conditions, these devices pose a fire risk.
The affected devices can be identified by their serial numbers, which are listed in the recall documentation. The source does not specify what actions consumers should take regarding this recall.
Written by software from the official notice below. Not reviewed by a lawyer.
Under certain conditions, there is a risk for fire.
Reason for recall: 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. Quantity: 67 devices Lot/code info: Devices with the following Serial Numbers: 120210000731, L2004034-154, 120210000716, L1905010-080, 120210000750, 120190000086, 120190001268, 120210000885, 120190000724, 120190001234 120190001276, 120210000732, L1911019-029, 120210000761, L2002011-094, 120210000747, 120210000760, 120210000730, 120210000734, 120190000076 120190000079, 120190000081, 120190000090, 120190000714, 120190000722, 120190000074, 120190000077, 120190000728, 120210001608, 120210000742, 120210000755, L2001006-040, 120210000733 L1911019-035, 120210000744, 120210001613, 120210001614, 120210000714 L1903102-021, 120190001269, 120210000743, 120210000741, L1912010-015, 120210000753, 120210000739, 120190000088, 120190000711, 120190000718 120190001264, 120210001615, L1903102-012, L2001016-045, 120190000078 120190000089, 120190001266, 120210000884, 120190000091, 120190000093, 120190000707, 120210000729, L1903103-006, L1912010-005 L1912013-033, L2002040-095, L2002040-064, L2002040-093, L2003004-106
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.