Class II — Potential Health Hazard

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

CMS8000 Patient Monitor Recalled by Contec Medical Systems Co., Ltd. Due to Patient monitor has nine identified cybersecurity vulnerabilities.

Date: April 10, 2025
Company: Contec Medical Systems Co., Ltd.
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 Contec Medical Systems Co., Ltd. directly.

Affected Products

CMS8000 Patient Monitor

Quantity: 7773

Why Was This Recalled?

Patient monitor has nine identified cybersecurity vulnerabilities.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Contec Medical Systems Co., Ltd.

Contec Medical Systems Co., Ltd. has 1 total recall tracked by RecallDetector.

Related Recalls

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