Class II — Potential Health Hazard

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

B105P Patient Monitor (with E-module slot option) Recalled by GE Medical Systems, LLC Due to GE Healthcare has become aware that if certain...

Date: November 16, 2022
Company: GE Medical Systems, LLC
Status: Ongoing
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 GE Medical Systems, LLC directly.

Affected Products

B105P Patient Monitor (with E-module slot option), REF 6160000-001-XXXXXX,

Quantity: 826 devices

Why Was This Recalled?

GE Healthcare has become aware that if certain B1x5P / B1x5M patient monitors use "mmHg" or "kPa" as the unit for CO2 measurement, the displayed value for CO2 measurement can be inaccurate when used in a location that is not at or near sea level.

Where Was This Sold?

Worldwide distribution.

About GE Medical Systems, LLC

GE Medical Systems, LLC has 146 total recalls tracked by RecallDetector.

Related Recalls

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