Ge Healthcare It
Complete recall history across all FDA and CPSC categories — 17 total recalls
Ge Healthcare It appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.
Device Recalls (17)
FDA medical device enforcement actions by Ge Healthcare It
| Date | Product | Reason | Class |
|---|---|---|---|
| Aug 26, 2013 | Merge Mammo is a multi-modality, vendor-neutral digital mammography workstati... | There is a potential safety issue with the 8.0.2 version software of the Merg... | Class II |
| Jun 11, 2013 | The Centricity PACS Workstation is intended for use as a primary diagnostic a... | GE has recently become aware of potential issues due to out of context issues... | Class II |
| Apr 19, 2013 | Centricity Enterprise Archive is a software product for receiving, archiving ... | GE Healthcare has become aware of a potential data loss issue associated with... | Class II |
| Mar 12, 2013 | The Centricity Laboratory System is intended to be an information system desi... | GE Healthcare has become aware of a potential safety issue associated with th... | Class II |
| Mar 12, 2013 | The Centricity Laboratory System is intended to be an information system desi... | GE Healthcare is aware of a potential safety issue with the use of GE Centric... | Class II |
| Mar 11, 2013 | Centricity Perinatal and Centricity Intensive Care is intended to be used in ... | 1) Under rare network conditions, a Centricity Perinatal process may maintain... | Class II |
| Feb 18, 2013 | Imagecast PACS with Centricity RIS-IC versions prior to 10.6 Update Package 1... | A software defect was discovered that causes images to be out of context with... | Class II |
| Nov 20, 2012 | The Centricity Laboratory System is intended to be an information system desi... | If environment variables MICRO_CORRECT_MSG_TYPE and CORRECT_MSG_TYPE are se... | Class II |
| Nov 20, 2012 | The Centricity Laboratory System is intended to be an information system desi... | GE Healthcare is aware of a potential safety issue associated with the use of... | Class III |
| Nov 20, 2012 | Centricity Laboratory Core Lab System 4.1 The Centricity Laboratory System... | The Centricity Laboratory removes free-text notes on a master panel when the ... | Class II |
| Nov 16, 2012 | Centricity Enterprise Archive is a software product for receiving, archiving ... | There is a potential for data loss associated with empty path names resulting... | Class II |
| Nov 15, 2012 | GE Centricity PACS Workstation, versions 3.1.1.x through 3.2.1.x Picture Ar... | While merging exams in a test instance, merges carry forward in the productio... | Class II |
| Oct 2, 2012 | Centricity Cardio Imaging 5.0 is a software only Picture Archiving and Commun... | GE Healthcare is aware of a potential safety risk where an image labeling sit... | Class II |
| Sep 15, 2012 | Centricity PACS System versions 3.X and higher and 4.X and higher Product Us... | There is a potential loss of image(s) associated with the Centricity to Centr... | Class II |
| Jun 15, 2012 | Centricity PACS IW by GE Healthcare Dynamic Imaging Solutions is a device tha... | Multiple issues were identified with the GE Centricity PACS-IW system that co... | Class II |
| Apr 19, 2012 | The GE Centricity Web; Software Version 3.0x, is intended for use under the d... | GE Healthcare has become aware of an issue associated with rejected images us... | Class II |
| Mar 4, 2011 | Imagecast PACS is an image management system intended to be used by trained p... | In Imagecast PACS versions prior to 3.6.51.01, the estimated magnification fa... | Class II |
Frequently Asked Questions
A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.
Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.
The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.
Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.
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