Hill-Rom Recalls Life2000 Ventilation Systems Due to Fire Risk

Plain-English summary

Hill-Rom Manufacturing, Inc. is recalling 67 units of the Life2000 Ventilation System, which includes the Life2000 Ventilator and Life2000 Compressor (Model MS-01-0118). The recall is due to a risk of fire under certain conditions. The devices are intended for use in home and institutional settings and are not intended for ambulance or air transport.

The affected devices were distributed nationwide in the United States, including in the states of AR, AZ, CA, DE, FL, IL, IN, KY, MN, NC, NM, NV, NY, OH, OK, TX, UT, VA, VT, and WI. Specific serial numbers for the affected units are listed in the official recall documentation.

Consumers and healthcare facilities should check their devices against the provided serial numbers. If a device is affected, users should follow the instructions provided by Hill-Rom or the FDA for remediation or replacement.

The recalled product

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.

Manufacturer

Hill-Rom Manufacturing, Inc.

Category

Medical Device — Ventilator

Hazard

• fire

Affected units

67

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Distribution

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