Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Critical RiskFDA Device
Medical Devices/Surgical Equipment

GE Carestation Anesthesia Systems Recalled for Unexpected Shutdown Risk

Agency Publication Date: December 18, 2025
Share:
Sign in to monitor this recall

Summary

GE Healthcare is recalling approximately 2,368 units of its Carestation 600 and 700 Series Anesthesia Systems and specific Power Management Board spare parts. Affected models include the Carestation 610, 620, 630, 650, 750, and 750c. These systems may unexpectedly shut down and reboot if the main power source is disconnected or fails, instead of switching to battery power as intended. If this occurs, mechanical ventilation and anesthesia delivery will be interrupted, and the device will not return to its previous settings after it reboots.

Risk

The failure of the device to switch to battery power during a power loss causes a system reboot, leading to a temporary stop in mechanical ventilation and anesthesia gas delivery. This disruption poses a critical risk to patients who rely on the machine for life-sustaining support during surgery.

What You Should Do

  1. This recall affects GE Healthcare Carestation anesthesia systems in the 600 and 700 series (including models 610, 620, 630, 650, 750, and 750c) and Power Management Board spare parts (FRU 2076139-001-S). See the Affected Products section below for the full list of affected codes.
  2. Stop using the recalled device immediately. Contact GE Medical Systems or your authorized distributor to arrange for a return, replacement, or professional correction of the power management board.
  3. Call the FDA Consumer Complaint hotline at 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls for additional information regarding this recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: GE Healthcare Carestation 600 Series Anesthesia System
Variants: Carestation 610 A1, Carestation 620 A1, Carestation 620 SE A1, Carestation 630 A1, Carestation 650 A1, Carestation 650 SE A1, Carestation 650c A1, Carestation 620 A2, Carestation 620 SE A2, Carestation 650 A2, Carestation 650 SE A2, Carestation 650c A2
Model / REF:
1012-9620-222
1012-9620-000
1012-9620-200
1012-9620-202
1012-9620-212
1012-9650-222
1012-9650-000
1012-9650-200
1012-9650-202
1012-9650-212
1012-9655-202
1012-9620-002
1012-9620-012
1012-9650-002
1012-9650-012
1012-9655-000
1012-9655-002
1012-9655-200
GTIN:
00195278626301
00840682103985
00195278439536
00195278626158
00195278626561
00195278626592
00840682103947
00195278439529
00195278626585
00195278625687
00195278625953
00840682124546
00195278569677
00840682124560
00195278569684
00840682103954
00840682124539
00195278439543

Recall #: Z-0913-2026; Quantity: 1277 units

Product: GE Healthcare Carestation 750 Series Anesthesia System
Variants: Carestation 750 A1, Carestation 750 A2, Carestation 750c A1, Carestation 750c A2
Model / REF:
1012-9750-000
1012-9750-002
1012-9755-000
1012-9755-002
GTIN:
00840682145596
00840682146470
00840682146425
00840682146463

Recall #: Z-0914-2026; Quantity: 888 units

Product: GE Healthcare Carestation anesthesia system Power Management Board (PMB) Field Replaceable Unit (FRU)
Model / REF:
2076139-001-S
Date Ranges: Distributed between June 2, 2025 and October 21, 2025

Recall #: Z-0915-2026; Quantity: 203 units

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98064
Status: Active
Manufacturer: GE Medical Systems China Co., Ltd.
Sold By: Authorized Medical Device Distributors; GE Healthcare Direct Sales
Manufactured In: China
Units Affected: 3 products (1277 units; 888 units; 203 units)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.