PlainRecalls

GE Medical Systems China Co., Ltd.

15 recalls on record · Latest: Dec 24, 2025

GE Medical Systems China Co., Ltd. Recall Insight

GE Medical Systems China Co., Ltd. appears on 15 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.018% of the federal archive — a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Dec 24, 2025, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 15 entries, severity tagging shows 12 critical, 3 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 15 of 15 entries — unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (15). The date window on this page runs from Sep 5, 2018 to Dec 24, 2025.

Manufacturer-level browsing is useful when monitoring a single firm for patterns — whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current — deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement — always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Critical Dec 24, 2025

GE Healthcare Carestation anesthesia system, product number and REF numbers: Carestation 610 A1, REF 1012-9620-222; Carestation 620 A1 REF 1012…

FDA Devices Critical Dec 24, 2025

GE Healthcare Carestation anesthesia system, product number and REF numbers: Carestation 750 A1, REF 1012-9750-000; Carestation 750 A2, REF 1012…

FDA Devices Moderate Jul 2, 2025

GE Healthcare LOGIQ F R3 Ultrasound System, Model/Catalog Number 5943263, diagnostic ultrasound system

FDA Devices Critical May 7, 2025

GE Healthcare CARESTATION 620 A2, Model/REF Number 1012-9620-002

FDA Devices Critical May 7, 2025

GE Healthcare CARESTATION 650C A1, Model/REF Number 1012-9655-000

FDA Devices Critical May 7, 2025

GE Healthcare CARESTATION 750 A2, Model/REF Number 1012-9750-002

FDA Devices Critical May 7, 2025

GE Healthcare Carestation 650 SE, Model/REF Number 1012-9650-012

FDA Devices Critical May 7, 2025

GE Healthcare Carestation 620 A1, Model/REF Number 1012-9620-200

FDA Devices Critical May 7, 2025

GE Healthcare CARESTATION 650 A2, Model/REF Number 1012-9650-002

FDA Devices Critical May 7, 2025

GE Healthcare CARESTATION 650C A2, Model/REF Number 1012-9655-002

FDA Devices Critical May 7, 2025

GE Healthcare Carestation 620 SE, Model/REF Number 1012-9620-012

FDA Devices Critical May 7, 2025

GE Healthcare CARESTATION 750c A2, Model/REF Number 1012-9755-002

FDA Devices Critical May 7, 2025

GE Healthcare CARESTATION 650 A1, Model/REF Number 1012-9650-000

FDA Devices Moderate Oct 11, 2023

F2-01 Frame, physiological patient monitor (with arrhythmia detection or alarms)

FDA Devices Moderate Sep 5, 2018

GE Carestation 620/650/650c, A1 and A2 (non-US distribution) anesthesia systems

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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Data Sources

  • Source: FDA + CPSC + NHTSA + USDA FSIS — federal recall filings naming this firm. Verify with FDA, CPSC, NHTSA, or USDA FSIS directly.
  • Source: PlainRecalls Manufacturer Index — firm-level aggregation across all four federal recall feeds