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.

201–225 of 276

ModerateFDA (Devices)·Z-2139-2014·2014-08-13
Ortho VITROS 3600 Immunodiagnostic System Software Recall
Ortho-Clinical Diagnostics is recalling VITROS 3600 systems due to a software defect that may associate incorrect patient demographics with sample IDs.
Product
VITROS 3600 Immunodiagnostic System --- For use in the in vitro quantitative, semi-quantitative and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents. The VITROS Software is a part of the VITROS 3600, 4600, & 5
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2141-2014·2014-08-13
Ortho-Clinical Diagnostics Recalls VITROS 5600 Systems Due to Software Error
Ortho-Clinical Diagnostics is recalling VITROS 5600 Integrated Systems because a software anomaly may associate incorrect patient demographics with sample IDs.
Product
VITROS 5600 Integrated System --- For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Chemistry Products Slides, VITROS Chemistry Products MicroTip Reagents and VITROS Immunodiagnostic Pr
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2121-2014·2014-08-06
McKesson Horizon Medical Imaging Software Recalled for Image Index Discrepancy
McKesson Medical Imaging is recalling Horizon Medical Imaging software due to a defect that may cause a mismatch between the expected image index and the actual folder content.
Product
Horizon Medical Imaging It is a medical image and information management application that is intended to receive, transmit, store, retrieve, display print and process digital medical images, digital medical video, and associated medical information from various medical imaging
Category
Medical Device
Distribution
48 states
ModerateFDA (Devices)·Z-2134-2014·2014-08-06
Brainlab Patient Data Manager 2.0 Software Recall for Image Display Defects
Brainlab AG is recalling Patient Data Manager 2.0 software due to defects in transferring and displaying non-square pixel medical images.
Product
Patient Data Manager 2.0 (Content manager 2.0, Patient Browser 4.0, DICOM Viewer 2.0) Brainlab Digital Lightbox. A system for the display of medical images. Model numbers 25100-05 and 25100-06. The software can transfer images to and from picture archiving and communicatio
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2075-2014·2014-07-23
Siemens syngo RT Dosimetrist 2.7 software update addresses data storage issue
Siemens Medical Solutions is updating syngo RT Dosimetrist 2.7 software to fix a safety issue where structure names were not stored correctly.
Product
Siemens syngo RT Dosimetrist 2.7 system Product Usage: The intended use of syngo Suite for Oncology Systems is as an accessory to the linear accelerator system to aid and support in the planning and delivery of x-ray radiation for the therapeutic treatment of cancer.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1944-2014·2014-07-09
Siemens syngo Lab Data Manager Software Recall for Configuration Errors
Siemens is recalling syngo Lab Data Manager software because configuration errors may cause test results to bypass manual review and release to the Laboratory Information System.
Product
syngo Lab Data Manager, SMN 10800057, 10803189, and 10804573.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1665-2014·2014-06-04
GE Healthcare Recalls Centricity PACS Workstation Due to Image Rejection Error
GE Healthcare is recalling 297 Centricity PACS Workstations because a software defect may cause images from previously displayed studies to be rejected unintentionally.
Product
The Centricity PACS Workstation is intended for use as a primary diagnostic and analysis tool for diagnostic images by trained healthcare professional, including radiologists, physicians, technologists, clinicians, and nurses. It is also intended for use as a clinical review work
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1646-2014·2014-05-28
Philips XIRIS 8.1.50.0 Recall Due to Patient Data Synchronization Error
Philips Healthcare Informatics is recalling 5 units of XIRIS 8.1.50.0 due to a synchronization error that may display incorrect patient information.
Product
Philips XRE, the dictation editor system included in the Philips XIRIS 8.1.50 XIRIS is a radiology information system (RIS) is a computer system that assist radiology services in the storing, manipulating and retrieving of patient information. This included patient scheduling
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1573-2014·2014-05-21
SCC Soft Computer Recalls SoftMic Laboratory Information System Software
SCC Soft Computer is recalling SoftMic version 4.0.7.0 because missing SNOMED codes may cause incomplete patient data and delayed treatment updates.
Product
SCC SA HIS version 4.0.7.0 when used with SoftMic version 4.0.7.0. SoftMic is a laboratory information system to be used in medical results, clinical, and public health laboratories by knowledgeable, trained, and experienced personnel. SoftMic enables the user to handle data
Category
Medical Device
Distribution
1 state
ModerateFDA (Devices)·Z-1504-2014·2014-04-30
Siemens ACUSON X700 Ultrasound Systems Recalled for Data Error
Siemens is recalling 490 ACUSON X700 ultrasound systems because previous patient data may replace current patient dates in reports.
Product
Siemens ACUSON X700 Ultrasound Systems with software version 1.0.00, 1.0.01, 1.0.02, 1.1.00 and 1.1.02. ultrasound imaging system.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1310-2014·2014-04-09
Technidata TDWorkstation Software Recalled for Potential Incorrect Patient Demography Transmission
Technidata S.A. is recalling TDWorkstation software versions 11.01.A and higher because a conflict may cause the system to send incorrect patient demography to connected instruments.
Product
TDWorkstation version 11.01.A or higher. TDWorkstation Evolution. TDWorkstation receives patient results from a connected instrument and sends them to a Laboratory Information System (LIS).
Category
Medical Device
Distribution
1 state
ModerateFDA (Devices)·Z-1299-2014·2014-04-02
Bio-Rad D-10 Hemoglobin Testing System Software Recall
Bio-Rad is recalling D-10 Hemoglobin Testing Systems because the software may occasionally generate duplicate results with incorrect sample identifiers.
Product
D-10" Hemoglobin Testing System, Model number: 220-0220 Manufactured by: Bio-Rad Laboratories, Inc. 4000 Alfred Nobel Drive Hercules, CA 94545 The D-10 Hemoglobin Testing System is a single module designed for hemoglobin analysis in mid-volume laboratories. The D-10 is
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1173-2014·2014-03-19
Horiba Medical Recalls ABX PENTRA ML Software Due to Data Transmission Bug
Horiba Medical is recalling ABX PENTRA ML software because a bug may transmit incorrect results to Laboratory Information Systems.
Product
Device Name: ABX PENTRA ML Model/Part #(s): A11A01652 Lot/Serial #(s): N/A Software Version(s): All versions are subject to this correction. Product Usage: The ABX PENTRA ML is a software data management system intended for use on ABX Hematology Analyzers.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1156-2014·2014-03-19
Mindray Recalls Panorama Central Station for Time Clock Data Lag
Mindray is recalling 732 Panorama Central Stations because Full Disclosure data and event indicators may lag behind the system time clock.
Product
Panaroma Central Station Product Usage: This device can view real time, store, print, graph, and trend patient clinical and demographic data. The device can also set independent alarm limits for data send by the bedside monitor.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1154-2014·2014-03-19
Clarity Medical Systems Recalls RetCam Devices Due to Age Calculation Error
Clarity Medical Systems is recalling RetCam 3, Portable, and Shuttle devices because a software error causes incorrect patient age calculations.
Product
RetCam 3, RetCam Portable and RetCam Shuttle; manufactured by Clarity Medical Systems, Inc.; Pleasanton, CA 94588. General ophthalmic imaging including retinal, corneal and external imaging.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1124-2014·2014-03-12
Medical Information Technology Recalls MEDITECH Microbiology Calculator Module
Medical Information Technology, Inc. is recalling MEDITECH Microbiology calculator modules due to a risk of patient results being removed from laboratory and electronic medical record systems.
Product
MEDITECH Microbiology - Calculator/data processing module, for clinical use.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1060-2014·2014-03-12
McKesson Anesthesia Care System Recalled for Data Mismatch
McKesson Technologies is recalling 10 units of the Anesthesia Care system because patient case data did not match the patient data, including data from another case.
Product
McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system is a computer based system which collects, processes,and records data both through manual entry and from monitors which themselves are attached to patients, such as in the operating room environment.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0976-2014·2014-02-19
McKesson Recalls Horizon Medical Imaging PACS Software Due to Archive Errors
McKesson Information Solutions LLC is recalling 618 units of Horizon Medical Imaging PACS software because images may be archived to incorrect locations, causing display failures.
Product
Horizon Medical Imaging, Picture Archive Communication System (PACS).
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0865-2014·2014-02-05
GE Centricity Laboratory System Software Recall for Calculation Errors
GE Healthcare is recalling Centricity Laboratory System software due to a defect that may report calculated results as 0 or truncate them.
Product
The Centricity Laboratory System is intended to be an information system designed to support the clinical and administrative activities associated with the provision and utilization of clinical laboratory services and facilities, e.g., the storing and delivering of analytical res
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0823-2014·2014-01-29
Siemens CentraLink Software Recall for Potential Patient Data Release Error
Siemens is recalling CentraLink Data Management System software versions 14.0.4, 14.0.5, and 14.0.8 because a disabled patient result may be released without proper review.
Product
Siemens CentraLink" Data Management System V14.0.4, V14.0.5 or V14.0.8 The CentraLink system software is a network solution provider and multi-system data manager for the instruments and lab automation systems (LAS) within the lab. The CentraLink software consolidates data fro
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-0580-2014·2014-01-01
EOS Imaging Recalls steroEOS Workstation Due to Data Copying Error
EOS Imaging is recalling 36 steroEOS Workstation units because a software error may prevent 3D model data from copying to clinical files and reports.
Product
steroEOS Workstation with software versions: 1.3, 1.4 and 1.5 used in processing 3D X-ray images Product Usage: The sterEOS Workstation is a general system for acceptance , transfer, display and digital processing of two 3D x-ray images.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0433-2014·2013-12-11
Siemens syngo Lab Data Manager Software Recall for Auto-verification Failures
Siemens Healthcare Diagnostics is recalling syngo Lab Data Manager software versions VA11B and VA12A because the system may release results that require manual review or delay result transmission.
Product
syngo(R) Lab Data Manager - Version VA11B and VA12A Systems Securely consolidates data from multiple lab instruments, the LIS and Siemens StreamLAB(R) Automation Solutions. It provides autoverification, integrated QC capabilities, browser-based connectivity supporting up to 25
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0242-2014·2013-11-20
Carestream Vue PACS Software Recall for Image Loading Issues
Carestream Health is recalling Vue PACS software because specific multi-slice images may fail to load in the viewer application.
Product
Carestream Vue PACS; UPG MX-O SVR 25K EX/YR UNLIMITED The CARESTREAM PACS is an image management system whose intended use is to provide completely scaleable local and wide area PACS solutions for hospital and related institutions/sites, which will archive, distribute, retrieve
Category
Medical Device
Distribution
26 states
ModerateFDA (Devices)·Z-0116-2014·2013-11-06
GE Centricity PACS Workstation Recalled for Workflow Interruption Issues
GE Healthcare is recalling 623 Centricity PACS Workstations due to software workflow interruptions that may prevent exams from closing correctly in the system.
Product
The Centricity PACS Workstation is intended for use as a primary diagnostic and analysis tool for diagnostic images by trained healthcare professionals, including radiologists, physicians, technologists, clinicians and nurses. It is also intended for use as a clinical review work
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0024-2014·2013-10-23
GE PET Discovery 610 and 710 Recalled for Image Series UID Conflict
GE Healthcare is recalling PET scanners because a software issue may cause different image series to share the same ID, potentially leading to incorrect image display.
Product
GE PET Discovery 610, PET Discovery 710. Intended for head and whole body attenuation corrected Positron Emission Tomography (PET) imaging.
Category
Medical Device
Distribution
Distributed nationwide