Home / Recalls / Hill-Rom Manufacturing, Inc. / Z-0484-2021

Z-0484-2021 Class II Terminated

Recalled by Hill-Rom Manufacturing, Inc. — Saint Paul, MN

FDA device recall Z-0484-2021 was initiated by Hill-Rom Manufacturing, Inc. on Nov 12, 2020 and is designated Class II. Reason for recall: Under certain conditions, there is a risk for fire. The recall status is terminated (terminated Nov 10, 2022). Affected quantity: 67 devices.

Recall details

Product Type: Devices
Report Date: Dec 2, 2020
Initiation Date: Nov 12, 2020
Termination Date: Nov 10, 2022
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 67 devices

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.

Distribution pattern

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.

Code information

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

Source

Dataset: openFDA device recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for Z-0484-2021
openFDA file date: Nov 10, 2026
Loaded by RegDataLab: Nov 11, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.