PlainRecalls

Ge Healthcare

Compiled from official public sources by the editorial team.

89 recalls on record · Latest: Mar 11, 2026

Ge Healthcare Recall Insight

Ge Healthcare appears on 89 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.088% 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 Mar 11, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 39 entries, severity tagging shows 1 critical, 38 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 39 of 39 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 (39). The date window on this page runs from Feb 12, 2014 to Jul 8, 2015.

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 Moderate Jul 8, 2015

GE Healthcare Innova IGS 630. Angiographic X-ray systems used in generating fluoroscopic and rotational images of human anatomy for diagnostic, in…

FDA Devices Moderate Jul 8, 2015

GE Healthcare Innova IGS 620. Angiographic X-ray systems used in generating fluoroscopic and rotational images of human anatomy for diagnostic, in…

FDA Devices Moderate Jul 8, 2015

GE Healthcare Discovery IGS 740 & GE Healthcare Innova IGS 740. Angiographic X-ray systems used in generating fluoroscopic and rotational images o…

FDA Devices Moderate Jul 8, 2015

GE Healthcare Innova 3100IQ. Angiographic X-ray systems used in generating fluoroscopic and rotational images of human anatomy for diagnostic, int…

FDA Devices Moderate Jul 8, 2015

GE Healthcare Innova IGS 540. Angiographic X-ray systems used in generating fluoroscopic and rotational images of human anatomy for diagnostic, in…

FDA Devices Moderate Jul 8, 2015

GE Healthcare Innova 3131IQ. Angiographic X-ray systems used in generating fluoroscopic and rotational images of human anatomy for diagnostic, int…

FDA Devices Moderate Jul 1, 2015

GE Healthcare, Treadmill T2100. For Exercise Testing, facilitating accurate blood pressure measurements and exercise testing within speed range of 0…

FDA Devices Moderate Jun 3, 2015

D-fend, (p/n 876446-HEL), and D-fend+ (p/n 881319-HEL) water trap. Used with Compact Airway Modules E/M-C(Ai)O(V)(X) and Cardiocap/5 monitors. Pr…

FDA Devices Moderate May 27, 2015

CT LightSpeed 16 and Discovery ST Pet/CT DST. Catalogue # 2339985. Designed to be a head and whole body CT scanner utilizing a new solid state det…

FDA Devices Moderate May 20, 2015

GE Healthcare, CARESCAPE Monitor B850, B650 and B450 (Bx50).

FDA Devices Moderate May 13, 2015

GE Discovery MR950 MRI system

FDA Devices Moderate May 6, 2015

GE Healthcare Automatic Mobile X-Ray (AMX) Series: Optima XR220 amx

FDA Devices Moderate May 6, 2015

GE Healthcare Automatic Mobile X-Ray (AMX) Series: Brivo XR285amx

FDA Devices Moderate May 6, 2015

GE Healthcare Automatic Mobile X-Ray (AMX) Series: Optima XR200 amx

FDA Devices Moderate Apr 22, 2015

Kenex Radiation Shield installed with GE Healthcare Interventional, Surgery, CT and X-Ray Imaging systems.

FDA Devices Moderate Apr 8, 2015

GE Healthcare, Aespire 7900, Aespire View Anesthesia Machines. Model numbers 1009-9012-000. Intended to provide general inhalation anesthesia and…

FDA Devices Moderate Apr 1, 2015

GE Healthcare, SIGNA 1.5T TWINSPEED, SIGNA INFINITY MRISYSTEM, SIGNA 3.0T INFINITY WITH EXCITE, SIGNA 3.0T WITH EXCITE, SIGNA EXCITE 1.5T, SIGNA EXCI…

FDA Devices Moderate Mar 25, 2015

GE Healthcare, Treadmill T2100 and Treadmill T2000 with power cord part numbers 408930-001 Rev E, 408930-002 Rev C, or 2028038-008 Rev B. Also Field …

FDA Devices Moderate Mar 25, 2015

GE Healthcare Engstrom Carestation, Engstrom Pro, Cart Only S/5 EC. GE model numbers 1505-8538-000, 1505-9000-000, and 1505-9003-000. Ventilators.

FDA Devices Moderate Mar 25, 2015

GE Healthcare Millennium VG, Discovery VH and VariCam Nuclear Medicine systems, all configurations. Product Usage: The intended use of the system…

FDA Devices Moderate Mar 18, 2015

GE Healthcare Proteus XR/a with wall stand model number 2260354. Intended for use in generating radiographic images of human anatomy in all genera…

FDA Devices Moderate Mar 4, 2015

The Centricity PACS Workstation is intended for use as a primary diagnostic and analysis tool for diagnostic images by trained healthcare professiona…

FDA Devices Critical Feb 25, 2015

This correction applies to all GE Healthcare MRI systems with superconducting magnets: Discovery MR450, Discovery MR750, Signa HDx, Signa HDxt, Signa…

FDA Devices Moderate Feb 4, 2015

The Revolution CT is a multi-slice (256 detector row) CT scanner consisting of a gantry, patient table, scanner desktop (operator console), system ca…

FDA Devices Moderate Jan 21, 2015

GE Healthcare, Proteus XR/a with wall stand model number 600-0301.

FDA Devices Moderate Jan 21, 2015

GE Healthcare, Discovery IGS 730 & Discovery IGS 740. Discovery IGS 730 : The angiographic X-ray systems are indicated for use in generating fluor…

FDA Devices Moderate Jan 21, 2015

GE Healthcare Revolution CT., multi-slice (256 detector row) CT scanner.

FDA Devices Moderate Jun 4, 2014

The Centricity PACS Workstation is intended for use as a primary diagnostic and analysis tool for diagnostic images by trained healthcare professiona…

FDA Devices Moderate May 14, 2014

Panda¿ iRes Infant Warmers integrated with Nellcor SpO2. Controlled infrared heat to neonates who are unable to thermo-regulate based on their own…

FDA Devices Moderate May 14, 2014

Panda¿ Freestanding Infant Warmers, integrated with Nellcor SpO2. Controlled infrared heat to neonates who are unable to thermo-regulate based on …

FDA Devices Moderate May 14, 2014

Giraffe¿ Infant Warmers integrated with Nellcor SpO2. Controlled infrared heat to neonates who are unable to thermo-regulate based on their own ph…

FDA Devices Moderate May 14, 2014

Nellcor SpO2 Upgrade kit, consists of a Nellcor SpO2 circuit board, an OEM part manufactured by a third party supplier; and an integral component of …

FDA Devices Moderate May 14, 2014

Panda¿ Wall-Mount Infant Warmers, integrated with Nellcor SpO2. Controlled infrared heat to neonates who are unable to thermo-regulate based on th…

FDA Devices Moderate Feb 12, 2014

Upgrade Kit, Resuscitation, T-Piece, part numbers M1139417, M1192226 and M1223628, labeled in part ***GE Healthcare 8880 Gorman Road Laurel, MD 20723…

FDA Devices Moderate Feb 12, 2014

Stand-Alone Resuscitation, T-Piece, part numbers 2063771-001, 2063772-001, 2063773-001, 2063774-001, 2063775-001, M1226442, M1241420, M1241421, M1241…

FDA Devices Moderate Feb 12, 2014

Stand-Alone Resuscitation Unit, Bag and Mask, part number M1226444, labeled in part ***GE Healthcare 8880 Gorman Road Laurel, MD 20723***www.gehealth…

FDA Devices Moderate Feb 12, 2014

Giraffe¿ Infant Warmers, part number M1118179, labeled in part *** GE Healthcare 8880 Gorman Road Laurel, MD 20723***www.gehealthcare.com* Giraffe…

FDA Devices Moderate Feb 12, 2014

Stand-Alone Resuscitation Unit, Bag and Mask, Upgrade Kits, part number M1139612, labeled in part ***GE Healthcare 8880 Gorman Road Laurel, MD 20723*…

FDA Devices Moderate Feb 12, 2014

Panda iRes¿ Infant Warmers, part number M1112198 and Panda Freestanding Warmers, part number 2063568, labeled in part *** GE Healthcare 8880 Gorman R…

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare Ge Healthcare with Zimmer Biomet, Inc. →

Data Sources

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

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.