Official recall record
GE Healthcare Carestation anesthesia system, product number and REF numbers: Carestation 610 A1, REF 1012-9620-222; Carestation 620 A1
- Issuing authority
- US FDA — Medical Devices
- Alert date
- 2025-11-14
- Country of alert
- China
- Alert level
- Class I
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00195278626301
- Brand on record
- GE Medical Systems China Co., Ltd.
What the authority reported
Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is unplugged or in the event of an AC mains power failure. Anesthesia systems only operate on battery power in a rare event that AC mains power is lost and there is no continuous backup emergency power. If AC power is interrupted, the system will not automatically switch over to the battery supply mode and will reboot. If this issue occurs, a temporary disruption of mechanical ventilation, manual ventilation, and volatile agent delivery may occur. Following the reboot, the system will not return to the previous ventilation settings.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Record last checked against the registry on 2026-05-31.
Other recalls from this brand
- 2025-05-16 · US FDA — Medical Devices
GE Healthcare LOGIQ F R3 Ultrasound System, Model/Catalog Number 5943263, diagnostic ultrasound system - 2025-03-21 · US FDA — Medical Devices
GE Healthcare CARESTATION 650 A2, Model/REF Number 1012-9650-002 - 2025-03-21 · US FDA — Medical Devices
GE Healthcare CARESTATION 750 A2, Model/REF Number 1012-9750-002