Life2000 Ventilation System — Class II medical device recall Z-0484-2021
Terminated recall by Hill-Rom Manufacturing, Inc., reported 2020-12-02, distributed nationwide. Under certain conditions, there is a risk for fire.
| Recall number | Z-0484-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hill-Rom Manufacturing, Inc., Saint Paul, MN, United States |
| Recall initiated | 2020-11-12 |
| Classified | 2020-11-24 |
| Reported by FDA | 2020-12-02 |
| Terminated | 2022-11-10 |
| Distributed | Nationwide (US) |
| Quantity | 67 devices |
| UPC / GTIN / UDI-DI | 00120190000076, 00120190000090, 00120190000724, 00120190001264, 00120210000734, 00120210000741 |
| Serial numbers | 120190000074, 120190000076, 120190000077, 120190000078, 120190000079, 120190000081, 120190000086, 120190000088, 120190000089, 120190000090, 120190000091, 120190000093, 120190000707, 120190000711, 120190000714, 120190000718, 120190000722, 120190000724, 120190000728, 120190001234, 120190001264, 120190001266, 120190001268, 120190001269, 120190001276 and 42 more |
| Model numbers | MS-01-0118 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0484-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.