Class II — Potential Health Hazard

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

Carestation 620 A1 Recalled by GE Healthcare, LLC Due to Carestation 620, 650 and 650c has Potential for...

Date: May 2, 2017
Company: GE Healthcare, LLC
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 GE Healthcare, LLC directly.

Affected Products

Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1

Quantity: 3,448 (334 US; 3,114 OUS)

Why Was This Recalled?

Carestation 620, 650 and 650c has Potential for Elevated FiCO2 and Unexpected System Malfunction

Where Was This Sold?

This product was distributed to 34 states: AL, AZ, AR, CA, CO, CT, FL, GA, ID, IL, IN, KY, LA, MD, MA, MI, MN, MS, MO, MT, NV, NH, NJ, NY, NC, OH, OK, PA, TN, TX, UT, VA, WA, WI

Affected (34 states)Not affected

About GE Healthcare, LLC

GE Healthcare, LLC has 474 total recalls tracked by RecallDetector.

Related Recalls

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