Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall 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.

U.S. FDA — Device Enforcement · United States · 2020-11-12 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0484-2021
Date of alert: 2020-11-12
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Hill-Rom Manufacturing, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 120210000731

Reported risk: Under certain conditions, there is a risk for fire.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall 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.

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