Hazard

Data Integrity Error recalls

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

What the numbers show

Total: 14
Critical: 0
Severe: 0
Most recent: 2023-05-10

Of the 14 data integrity error recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) 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 error 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.

1–14 of 14

HighFDA (Devices)·Z-1500-2023·2023-05-10
GE Healthcare radiological imaging system patient information mismatch
GE Healthcare's Centricity PACS-IW radiological imaging system can mismatch patient information when correcting study details. 17 units distributed worldwide are affected.
Product
Centricity PACS-IW with Universal Viewer, Model/Catalog Numbers: a) 2066908-061, b) 2066908-077, c) 2066908-086, d) 2066908-111, e) 2066908-123, f) 2066908-136, g) 2066908-150; Radiological Image Processing System
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-1560-2021·2021-05-19
Haag-Streit LENSTAR LS900 Software Recall for Data Mixing Errors
Haag-Streit USA Inc is recalling Eyesuite 9.3.1 software for LENSTAR LS900 devices due to potential mixing of patient names and examination data.
Product
Eyesuite 9.3.1 software, LENSTAR, MODEL LS900: ac-powered slit-lamp biomicroscope.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2747-2020·2020-08-12
Siemens DCA Vantage Barcode Scanner Recalled for Data Integrity Issues
Siemens Healthcare is recalling 1,800 DCA Vantage Handheld Barcode Scanners because they may fail to verify check digits or incorrectly process barcodes, potentially leading to data errors.
Product
DCA Vantage Handheld Barcode Scanner - Zebra Model - Model # DS4308 - HC0015BZZWW external accessory to DCA Vantage Analyzer US
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1540-2017·2017-03-29
Hitachi Oasis MRI System Recalled for Image Data Transfer Errors
Hitachi Medical Systems America Inc is recalling 210 Hitachi Oasis MRI Systems because image data transferred to workstations showed errors on the slice position reference image.
Product
Hitachi Oasis MRI System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0695-2016·2016-02-03
Bio-Rad D-10 Rack Loader Recalled for Potential Sample ID Error
Bio-Rad is recalling D-10 Rack Loaders because a rare configuration issue could assign patient results to incorrect sample IDs.
Product
D-10 Rack Loader; Model Number 220-0600; Hematology: The D-10 is a fully integrated system for sample dilution, processing and analysis of hemoglobin, designed for use with specific Bio-Rad reagent kits. The D-10 incorporates the use of a dedicated software system for instrum
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0425-2016·2015-12-23
bioMerieux MYLA Clinic Patch 3.2.0 CD Recall for Patient Data Linking Error
bioMerieux, Inc. is recalling MYLA Clinic Patch 3.2.0 CD software because it may link test results to incorrect patient records when connected to specific laboratory systems.
Product
MYLA CLINIC PATCH 3.2.0 CD Product Usage: MYLA is a computer application (Middleware) based on Web 2.0 technology which: Interfaces between the instruments connected to the application and the LIS(s) (Laboratory Information System(s)).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2716-2014·2014-10-08
Siemens Recalls ADVIA Centaur XP Immunoassay Systems Due to Data Error
Siemens Healthcare Diagnostics is recalling ADVIA Centaur XP Immunoassay Systems because patient demographic data may incorrectly merge with subsequent orders under rare circumstances.
Product
ADVIA Centaur XP Immunoassay System (including refurbished units), This system is intended for professional use in a laboratory environment only. Tests performed using this system are intended for in vitro diagnostic use. As with all diagnostic tests, a definitive clinical di
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-2715-2014·2014-10-08
Siemens Recalls ADVIA Centaur Immunoassay Systems Due to Data Error
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Immunoassay Systems because patient demographic data may be incorrectly merged under rare circumstances.
Product
ADVIA Centaur Immunoassay System (including refurbished units), This system is intended for professional use in a laboratory environment only. Tests performed using this system are intended for in vitro diagnostic use. As with all diagnostic tests, a definitive clinical diagn
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-0271-2014·2013-11-20
Siemens syngo.plaza Image Processing System Recalled for Patient Data Merge Error
Siemens is recalling 19 syngo.plaza image processing systems because a software function can cause unintended patient data merges when transferring data between systems.
Product
Siemens syngo.plaza image processing system image processing radiological system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1950-2013·2013-08-21
Veridex CellTracks Analyzer II Recalled for Patient Data Association Error
Veridex is recalling CellTracks Analyzer II software versions 2.5.1 and below because patient demographics were incorrectly associated with another patient's ID.
Product
CELLTRACKS ANALYZER II (Software Version 2.5.1 & Below. Product Usage: The CELLTRACKS AUTOPREP System is a general purpose laboratory instrument used with immunomagnetic reagents that capture and enrich target cells, and labeling reagents that differentiate cells in whole b
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1949-2013·2013-08-21
Veridex CellTracks AutoPrep System Recalled for Patient Data Mismatch
Veridex is recalling CellTracks AutoPrep System software due to a reported error where patient demographics were incorrectly associated with another patient's ID.
Product
CELLTRACKS AUTOPREP System (Software Version 2.4.1 & Below. Product Usage: The CELLTRACKS AUTOPREP System is a general purpose laboratory instrument used with immunomagnetic reagents that capture and enrich target cells, and labeling reagents that differentiate cells in who
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0989-2013·2013-04-03
Biomerieux VITEK 2 60 Computer System Recalled for Data Linking Error
Biomerieux Inc is recalling VITEK 2 60 computer systems due to a potential error that could link test results to the wrong patient.
Product
VITEK 2 60 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
ModerateFDA (Devices)·Z-2332-2012·2012-09-19
Sunquest Laboratory Software Recalled for Patient Data Merge Errors
Sunquest Information Systems is recalling specific versions of its Laboratory software because a merge function may cause receiving systems to incorrectly merge patient data.
Product
Sunquest Laboratory Sunquest Laboratory is intended for use by professionals working in a clinical laboratory. Sunquest Laboratory is intended for use only by professionals who have received extensive training in the use of the software. Sunquest Laboratory is controlled via u
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2163-2012·2012-08-15
Radiometer ABL Software Recall for HL7 Data Transmission Errors
Radiometer America Inc. is recalling ABL software version 6.12 for ABL800 and ABL700 analyzers because HL7 2.5 data transmission errors can mix up queued results.
Product
The ABL software version 6.12 for the ABL800 and ABL700 analyzer. The analyzers are intended for the in Vitro testing of: -Samples of whole blood for the parameters pH, pO2, pCO2, cK+, cNa+, cCa2+, cCl-, cGlu, cLac, cCrea, ctBil, and co-oximetry parameters (ctHb, sO2, and the
Category
Medical Device
Distribution
Distributed nationwide