Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Breas Vivo 50 Home Care Ventilator Product Usage: Respiratory Care Recalled by Breas Medical AB Due to Unintended treatment termination could result from a keypad...

Date: November 7, 2014
Company: Breas Medical AB
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Breas Medical AB directly.

Affected Products

Breas Vivo 50 Home Care Ventilator Product Usage: Respiratory Care

Quantity: 846 US

Why Was This Recalled?

Unintended treatment termination could result from a keypad malfunction in some situations. The device erroneously interprets this as a Stop Treatment Instruction. An alarm will not sound, or be registered. Accessories and monitoring equipment connected to the Vivo 50 will stop functioning as the device enters stand-by mode.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Breas Medical AB

Breas Medical AB has 1 total recall tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report