PlainRecalls

Ge Healthcare It

Compiled from official public sources by the editorial team.

17 recalls on record · Latest: Sep 14, 2016

Ge Healthcare It Recall Insight

Ge Healthcare It appears on 17 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.017% 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 Sep 14, 2016, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 17 entries, severity tagging shows 0 critical, 16 moderate, and 1 lower-severity recalls. Affected-unit counts are disclosed on 17 of 17 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 (17). The date window on this page runs from Jul 3, 2013 to Sep 14, 2016.

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 Sep 14, 2016

Centricity Enterprise Archive is a software product for receiving, archiving and sending of medical data. Qualified system administrators install, mo…

FDA Devices Moderate Sep 7, 2016

Centricity Laboratory Core Lab System 4.1 The Centricity Laboratory System is intended to be an information system designed to support the clinica…

FDA Devices Moderate Aug 24, 2016

GE Centricity PACS Workstation, versions 3.1.1.x through 3.2.1.x Picture Archiving and Communication System Used as a primary diagnostic and ana…

FDA Devices Moderate Aug 3, 2016

Imagecast PACS with Centricity RIS-IC versions prior to 10.6 Update Package 18 Product Usage: is an image management system intended to be used by …

FDA Devices Moderate Dec 31, 2014

Centricity Enterprise Archive is a software product for receiving, archiving and sending of medical data. DICOM devices (e..g. modalities, workstatio…

FDA Devices Low Feb 5, 2014

The Centricity Laboratory System is intended to be an information system designed to support the clinical and administrative activities associated wi…

FDA Devices Moderate Jan 22, 2014

Centricity PACS System versions 3.X and higher and 4.X and higher Product Usage: The Centricity PACS Workstation is intended for use as a primary d…

FDA Devices Moderate Jan 22, 2014

Merge Mammo is a multi-modality, vendor-neutral digital mammography workstation that enables imaging centers to use a single workstation to display a…

FDA Devices Moderate Jan 22, 2014

Imagecast PACS is an image management system intended to be used by trained professionals, including but not limited to physicians, nurses and medica…

FDA Devices Moderate Jan 8, 2014

The Centricity Laboratory System is intended to be an information system designed to support the clinical and administrative activities associated wi…

FDA Devices Moderate Dec 11, 2013

The GE Centricity Web; Software Version 3.0x, is intended for use under the direct supervision of a licensed healthcare practitioner. The Centricity …

FDA Devices Moderate Nov 27, 2013

The Centricity Laboratory System is intended to be an information system designed to support the clinical and administrative activities associated wi…

FDA Devices Moderate Nov 27, 2013

Centricity Perinatal and Centricity Intensive Care is intended to be used in clinical departments healthcare delivery systems such as a Labor and Del…

FDA Devices Moderate Nov 6, 2013

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 Nov 6, 2013

Centricity PACS IW by GE Healthcare Dynamic Imaging Solutions is a device that receives medical images (including mammograms) and data from various i…

FDA Devices Moderate Oct 30, 2013

Centricity Cardio Imaging 5.0 is a software only Picture Archiving and Communication System (PACS). Product Usage: It will be sold as a softwa…

FDA Devices Moderate Jul 3, 2013

The Centricity Laboratory System is intended to be an information system designed to support the clinical and administrative activities associated wi…

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare Ge Healthcare It 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.