Hazard

Data Integrity recalls

276 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total: 276
Critical: 0
Severe: 9
Most recent: 2026-08-19

Of the 276 data integrity recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 9 (3%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all data integrity recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

226–250 of 276

ModerateFDA (Devices)·Z-0023-2014·2013-10-23
GE Optima CT660 Recalled for Potential Series UID Generation Error
GE Healthcare is recalling Optima CT660 scanners because the DMPR and Screen Save functions may generate duplicate Series UIDs, potentially causing PACS systems to combine patient series incorrectly.
Product
GE, Optima CT660. Intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2276-2013·2013-10-02
Elekta Monaco Radiation Treatment Planning System Software Recall
Elekta is recalling Monaco RTP System software versions 3.10.00 and later because an upgrade script may overwrite treatment couch files with incorrect default values.
Product
Monaco RTP System Radiation treatment planning
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2266-2013·2013-10-02
GE Healthcare Recalls MRI Scanners Due to Non-Unique Series Identifiers
GE Healthcare is recalling specific MRI scanners because they may generate non-unique series identifiers in image headers, which can cause data association errors when exported to PACS systems.
Product
GE 1.5T Signa HDxt, 3.0T Signa HDxt, Signa Vibrant, HD23 Software and the following model numbers: 2395001, 2395001-2, 2395001-3, 2395001-4, 5269997-2, 5269997-4, 2377062-61, 5127452-3, 5127452, 5337894-3, 5337894-4, 5911000-4, 5911000-5, 53085735308573-2. GE Discovery MR750w
Category
Medical Device
Distribution
5 states
HighFDA (Devices)·Z-1931-2013·2013-08-14
Mitsubishi VERO Linear Accelerator Software Recall for Data Storage Error
Mitsubishi Heavy Industries is recalling VERO Linear Accelerator Systems due to a software anomaly that may save treatment records to the wrong location.
Product
MHI-TM2000 Linear Accelerator System, Software Version 3.0.0 revision 13 or earlier; Proprietary and Trade Name: MHI-TM2000/ VERO (TM); Common Name: Medical Linear Accelerator. MHI-TM2000 Linear Accelerator System is intended for radiation therapy of lesions, tumors and cond
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1912-2013·2013-08-14
BioMerieux Vitek 2 Software Recall for Antibiotic Code Errors
BioMerieux is recalling Vitek 2 software version 6.01 because antibiotic codes for three specific drugs are not updated properly when interfaced with Laboratory Information Systems.
Product
bioMerieux Vitek 2 Systems Software version 6.01 software, used with the VITEK 2 automated system. Kit, UPDT V2S 6.01 ES. Part number: 414561. The product is used with the VITEK 2 automated system which consists of instruments, software and reagent cards designed for the iden
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1917-2013·2013-08-14
BioMérieux Vitek 2 Software Recall for Antibiotic Code Errors
BioMérieux is recalling Vitek 2 software version 6.01 because specific antibiotic codes are not updated correctly when interfaced with Laboratory Information Systems.
Product
bioMerieux Vitek 2 Systems Software version 6.01 software, used with the VITEK 2 automated system. Kit, UPDT V2S 6.01 PT. Part number: 414566. The product is used with the VITEK 2 automated system which consists of instruments, software and reagent cards designed for the iden
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1909-2013·2013-08-14
BioMerieux Vitek 2 Software Recall for Antibiotic Code Errors
BioMerieux is recalling Vitek 2 software version 6.01 because specific antibiotic codes were not updated correctly during an upgrade, potentially affecting laboratory reporting.
Product
bioMerieux Vitek 2 Systems Software version 6.01 software, used with the VITEK 2 automated system. Kit, UPDT V2S 6.01ML2. Part number: 414538. The product is used with the VITEK 2 automated system which consists of instruments, software and reagent cards designed for the iden
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1918-2013·2013-08-14
BioMérieux Vitek 2 Software Recall for Antibiotic Code Errors
BioMérieux is recalling Vitek 2 Systems Software version 6.01 because specific antibiotic codes are not updated properly when interfaced with Laboratory Information Systems.
Product
bioMerieux Vitek 2 Systems Software version 6.01 software, used with the VITEK 2 automated system. Kit, UPDT V2S 6.01 DA, SV. Part number: 414567. The product is used with the VITEK 2 automated system which consists of instruments, software and reagent cards designed for the
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1907-2013·2013-08-14
BioMérieux Vitek 2 Software Version 6.01 Recalled for Interface Errors
BioMérieux is recalling Vitek 2 Systems Software version 6.01 because antibiotic codes for three specific drugs are not updated properly when interfaced with Laboratory Information Systems.
Product
bioMerieux Vitek 2 Systems Software version 6.01 software, used with the VITEK 2 automated system. Kit, V2S 6.01 RP5800-WES7 Media. Part number: 413861. The product is used with the VITEK 2 automated system which consists of instruments, software and reagent cards designed fo
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1916-2013·2013-08-14
BioMerieux Vitek 2 Software Version 6.01 Recalled for Interface Errors
BioMerieux is recalling Vitek 2 software version 6.01 because antibiotic codes for Cefovecin, Prulifloxacin, and Ceftaroline are not updated properly when interfaced with Laboratory Information Systems.
Product
bioMerieux Vitek 2 Systems Software version 6.01 software, used with the VITEK 2 automated system. Kit, UPDT V2S 6.01 NO. Part number: 414565. The product is used with the VITEK 2 automated system which consists of instruments, software and reagent cards designed for the iden
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1920-2013·2013-08-14
BioMerieux Vitek 2 Software Version 6.01 Recalled for Interface Errors
BioMerieux Inc is recalling Vitek 2 Systems Software version 6.01 because antibiotic codes for three specific drugs are not updated correctly when interfacing with Laboratory Information Systems.
Product
bioMerieux Vitek 2 Systems Software version 6.01 software, used with the VITEK 2 automated system. Kit, UPDT V2S 6.01 ZH. Part number: 414569. The product is used with the VITEK 2 automated system which consists of instruments, software and reagent cards designed for the iden
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1911-2013·2013-08-14
BioMerieux Vitek 2 Software Recall for Antibiotic Code Errors
BioMerieux is recalling Vitek 2 software version 6.01 because specific antibiotic codes are not updated correctly when interfaced with Laboratory Information Systems.
Product
bioMerieux Vitek 2 Systems Software version 6.01 software, used with the VITEK 2 automated system. Kit, UPDT V2S 6.01 EN. Part number: 414560. The product is used with the VITEK 2 automated system which consists of instruments, software and reagent cards designed for the iden
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1915-2013·2013-08-14
BioMérieux Vitek 2 Software Recall Due to Antibiotic Code Errors
BioMérieux is recalling Vitek 2 software version 6.01 because antibiotic codes for three drugs are not updated correctly when interfaced with laboratory systems.
Product
bioMerieux Vitek 2 Systems Software version 6.01 software, used with the VITEK 2 automated system. Kit, UPDT V2S 6.01 JA. Part number: 414564. The product is used with the VITEK 2 automated system which consists of instruments, software and reagent cards designed for the iden
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1908-2013·2013-08-14
BioMerieux Vitek 2 Software Recall for Interface Code Errors
BioMerieux is recalling Vitek 2 software version 6.01 because antibiotic codes for three specific drugs were not updated correctly during the software upgrade.
Product
bioMerieux Vitek 2 Systems Software version 6.01 software, used with the VITEK 2 automated system. Kit, UPDT V2S 6.01ML1. Part number: 414537. The product is used with the VITEK 2 automated system which consists of instruments, software and reagent cards designed for the iden
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1849-2013·2013-08-07
GE Healthcare Recalls LOGIQ e Ultrasound Systems for Patient Data Linking Error
GE Healthcare is recalling 588 LOGIQ e ultrasound systems because image data from one patient may be linked to another patient's ID.
Product
GE Healthcare, LOGIQ e Ultrasound System. The LOGIQ i/e and Vivid e is a general purpose ultrasound system intended for use by a qualified physician for evaluation by ultrasound imaging or fluid flow analysis of the human body. Specific clinical applications and exam types in
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1365-2013·2013-05-29
Medical Information Technology Recalls Bi-Directional Communication Analyzer Interface
Medical Information Technology, Inc. is recalling 56 MEDITECH Bi-Directional interactive Communication Analyzer Interface devices due to incorrect transmission of laboratory results.
Product
MEDITECH Bi-Directional interactive Communication Analyzer Interface; Integrates with MEDITECH's Laboratory Information System (LIS) with Other Vendor systems to manage the transfer of patient results and demographic information.
Category
Medical Device
Distribution
1 state
ModerateFDA (Devices)·Z-1345-2013·2013-05-29
Technidata TD-Synergy Laboratory Information System Software Recall
Technidata is recalling TD-Synergy Laboratory Information System software because a specific keyboard shortcut can modify previously entered test results.
Product
TD-Synergy. Laboratory Information System.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1338-2013·2013-05-29
Philips CT Systems Recall for Incorrect CTDIVol Data Storage
Philips is recalling 515 CT systems because they stored the sum of CTDIVol values instead of individual slice values, resulting in incorrect data.
Product
Brilliance CT 16-Slice Water, System Code: 728245; Brilliance CT 10-Slice Water, System Code: 728250; Brilliance CT 6-Slice Water, System Code: 728255; MX8000 IDT 16, System Code: 728120 & MX8000 IDT 10, System Code: 728125 Computed Tomography X-ray systems. Distributed by Phil
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1339-2013·2013-05-29
Boston Scientific Recalls LATITUDE Patient Management System Software
Boston Scientific is recalling the LATITUDE Patient Management System software because a system update caused clinic faxes to display illegible characters instead of required patient information.
Product
LATITUDE¿ Patient Management System, Model 6488, Version 7.3. The LATITUDE Patient Management system is intended for use to remotely communicate with a compatible Boston Scientific pulse generator and transfer data to a central database.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1105-2013·2013-04-24
Siemens syngo WorkFlow SLR Recall for Patient Data Display Error
Siemens Medical Solutions is recalling syngo WorkFlow SLR software due to a defect that may display the wrong patient's documents in signed reports.
Product
Siemens syngo WorkFlow SLR, Radiological Information System, Version VA31A SP1/SP2/SP3 The information system syngo(R) Workflow SLR is a digital radiology information system (RIS) with integrated modules for patient administration, examination, reporting, statistics and syste
Category
Medical Device
Distribution
31 states
HighFDA (Devices)·Z-1137-2013·2013-04-24
GE Healthcare AW Server Recalled for Patient Data Display Error
GE Healthcare is recalling AW Server software due to a defect where patient data from one individual may be displayed in the Results Viewer for a different patient.
Product
GE Healthcare, AW Server. Product Usage: . AW Server is a medical software system that allows multiple users to remotely access AW applications from compatible computers on a network. The system allows networking, selection, processing and filming of multimodality DICOM image
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1070-2013·2013-04-17
AGFA IMPAX CV Software Recall for Incorrect Data Transfer
AGFA Corp. is recalling 26 units of IMPAX CV software because baseline pulmonary capillary wedge pressure values were not correctly transferring into hospital electronic health records.
Product
IMPAX CV Reporting Cardiac Catheterization module and IMPAX CV Outbound Reporting. Facilitates digital reports for catheterization, echocardiography, and congenital heart disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0990-2013·2013-04-03
Biomerieux VITEK 2 XL Computer System Recalled for Patient Data Linking Errors
Biomerieux Inc. is recalling VITEK 2 XL computer systems equipped with specific Hewlett-Packard PCs due to a potential risk of linking test results to the wrong patient.
Product
VITEK 2 XL computer system when equipped with the following Hewlett-Packard PC models: (1) rp5700, Cat. #W0452; (2) rp5700 (refurbished), Cat. #W0452R; (3) rp5800 XPE, Cat. 413642; (4) rp5800 WES7, Cat. #413862; (5) dc7100 8-port, Cat. #W0441; (6) dc7100 8-port (refurbis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0991-2013·2013-04-03
Biomerieux VITEK 2 Compact Computer System Recall for Patient Data Error
Biomerieux Inc. is recalling VITEK 2 Compact computer systems because a software issue could link test results to the wrong patient.
Product
VITEK 2 Compact computer system when equipped with the following Hewlett-Packard PC models: (1) dc7100 8-port, Cat. #W0441; (2) dc7100 8-port (refurbished), Cat. #W0441R; (3) dc7700 8-port, Cat. #W0447; (4) dc7700 8-port (refurbished), Cat. #W0447R; (5) dc7800, Cat. #W
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0935-2013·2013-03-20
GE Healthcare Recalls MRI Systems Due to Reporting Tool Error
GE Healthcare is recalling multiple MRI systems because an error in the SR Viewer Reporting Tool allows edits to be saved to incorrect reports.
Product
Optima MR450w, Discovery MR450, Discovery MR750, Signa HDx, Signa HDxt, Signa HDi, Signa Vibrant, and GE 1.5T Signa HDe MR System. The GE Signa HDx MR system is a whole body magnetic resonance scanner.
Category
Medical Device
Distribution
2 states