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 Medical Systems China Co., Ltd. Due to Possible incomplete seal between the CO2 absorber and...
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 China Co., Ltd. directly.
Affected Products
Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1
Quantity: 5,148 devices
Why Was This Recalled?
Possible incomplete seal between the CO2 absorber and the breathing circuit CO2 bypass port assembly of the Carestation 600 Series systems.
Where Was This Sold?
This product was distributed to 38 states: AL, AZ, AR, CA, CO, CT, DE, 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, VT, VA, WA, WV, WI, DC
About GE Medical Systems China Co., Ltd.
GE Medical Systems China Co., Ltd. has 26 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report