Hazard

Data Loss recalls

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

What the numbers show

Total: 106
Critical: 0
Severe: 5
Most recent: 2026-08-12

Of the 106 data loss recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 5 (5%) 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 loss 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.

76–100 of 106

ModerateFDA (Devices)·Z-1670-2015·2015-06-03
Siemens Uroskop Omnia Max X-Ray System Software Data Loss Recall
Siemens is recalling 133 Uroskop Omnia Max X-ray systems due to software defects that cause image deletion and connection issues.
Product
SIEMENS Uroskop Omnia Max ; a solid state detector fluoroscopic X-Ray system, primarily for urological applications (functional x-ray diagnostic, endourology and minimal invasive urology/surgery). The system,, which includes a radiologic/urologic treatment table, may be used for
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1667-2015·2015-06-03
Siemens Ysio Max Radiographic System Recalled for Software Data Loss
Siemens is recalling 133 Ysio Max radiographic systems because a software defect can delete acquired images and studies, requiring patients to repeat exposures.
Product
SIEMENS Ysio Max; a radiographic system used in hospitals, clinics, and medical practices. Ysio Max enables radiographic and tomographic exposures of the whole body including: skull, chest, abdomen, and extremities and may be used on pediatric, adult and bariatric patients. It c
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1574-2015·2015-05-13
MHI-TM2000 Linear Accelerator System Software Recall for Communication Errors
Mitsubishi Heavy Industries is recalling 11 MHI-TM2000 Linear Accelerator Systems due to a software defect that allows radiation delivery despite communication errors and prevents saving treatment records.
Product
MHI-TM2000 Linear Accelerator System (Software Version 3.5.0 and 3.5.1)
Category
Medical Device
Distribution
4 states
ModerateFDA (Devices)·Z-1584-2015·2015-05-13
Siemens ACUSON SC2000 Ultrasound Systems Recalled for Image Loss
Siemens Medical Solutions USA is recalling 476 ACUSON SC2000 ultrasound systems because post-exercise images may be lost during Stress Echo procedures.
Product
ACUSON SC2000 ultrasound systems at software versions VA20A or VA20B. Model number 10433816. The SC2000 ultrasound imaging system is intended for the following applications: Cardiac, Neo-natal and Fetal Cardiac, Pediatric, Transespohageal, Adult Cephalic, Peripheral Vessel, A
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1144-2015·2015-03-04
Spacelabs XPREZZON Bedside Monitors Recalled for Boot Failure
Spacelabs Healthcare is recalling XPREZZON Bedside Monitors because they may fail to boot up or reset to factory defaults after power on.
Product
Spacelabs Healthcare XPREZZON Bedside Monitor, Model 91393. The Spacelabs Healthcare XPREZZON Bedside Monitor passively displays data generated by Spacelabs parameter modules, Flexport interfaces, and other Spacelabs SDLG based products as waveform and numeric displays, trends a
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-1214-2015·2015-03-04
GE Healthcare Recalls Centricity PACS Workstation Due to Exam Merge Failure
GE Healthcare is recalling 128 Centricity PACS Workstation systems because a software defect may cause exam records to go missing in single Study Mode.
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
ModerateFDA (Devices)·Z-1027-2015·2015-02-04
Siemens Syngo.plaza PACS Recalled for Potential Image Loss During System Crashes
Siemens Medical Solutions is recalling 50 Syngo.plaza PACS systems because images may be lost if the system crashes before saving data to the hard disk.
Product
Syngo.plaza: Syngo.plaza is a Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images. It supports the physician in diagnosis and treatment planning. Syngo.plaza also suppor
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0833-2015·2014-12-31
GE Healthcare Recalls Centricity Enterprise Archive Software Due to Data Loss Risk
GE Healthcare is recalling Centricity Enterprise Archive software versions 4.0.x due to a potential data loss issue associated with HL-7 updates.
Product
Centricity Enterprise Archive is a software product for receiving, archiving and sending of medical data. DICOM devices (e..g. modalities, workstations) Communicate with the archive using the DICOM protocol (published by ACR-NEMA). The clinical use is limited to the interaction t
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2180-2014·2014-08-20
Siemens Syngo RT Software Recalled for Sporadic System Crashes
Siemens is recalling Syngo RT Therapist and Oncologist software versions 4.3.SP1 due to sporadic system crashes that prevent unloading patient data.
Product
Siemens Syngo RT Therapist and Syngo RT Oncologist intended use of the SIEMENS branded Syngo RT Therapist and Syngo RT Oncologist software applications used with SIEMENS family of linear accelerator systems is to deliver X-Ray photon and electron radiation for the therapeutic tre
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-2085-2014·2014-07-30
GE Healthcare CARESCAPE Patient Monitors Recalled for Data Loss
GE Healthcare is recalling CARESCAPE B850, B650, and B450 patient monitors because the Patient Data Module may fail to communicate, causing partial loss of monitoring parameters.
Product
GE Healthcare, CARESCAPE Monitor B850, B650 or B450. Patient Monitor.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1846-2014·2014-07-02
ProBeam Proton Therapy System Recalled for Treatment History Data Loss
Varian Medical Systems is recalling ProBeam Proton Therapy Systems because the Treatment Control and Monitoring application may fail to send treatment history records to the ARIA database.
Product
ProBeam Proton Therapy System (HGA and HFB) Product Usage:ProBeam Proton Therapy System provides protons for precision radiotherapy of lesions, tumors, and conditions anywhere in the body. where radiation treatment is indicated.
Category
Medical Device
Distribution
1 state
ModerateFDA (Devices)·Z-1622-2014·2014-05-28
Siemens syngo Imaging XS Software Recall Due to Data Deletion Risk
Siemens Medical Solutions is recalling 64 syngo Imaging XS systems because a software change may have caused the deletion of archived medical images.
Product
syngo Imaging XS Syngo Imaging XS is a Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images. It supports the physician in diagnosis and treatment planning. Syngo Imaging
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1569-2014·2014-05-14
Shimadzu Digital Radiography X-Ray System Recalled for Image Loss
Shimadzu Medical Systems is recalling its Digital Radiography X-Ray System because a report was received regarding lost images under certain circumstances.
Product
Shimadzu Digital Radiography X-Ray System, Catalog No. DAR-8000f. This device is intended to be used for radiography in the hospital with X-ray devices.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0927-2014·2014-02-12
GE Healthcare Recalls CARESCAPE Monitor B850 Due to Communication Loss
GE Healthcare is recalling 12,945 CARESCAPE Monitor B850 units worldwide because the F5-01 Frame may lose communication with the patient monitor.
Product
CARESCAPE Monitor B850, a multi-parameter high acuity patient monitor intended for use in multiple areas within a professional healthcare facility. Product Usage: The CARESCAPE Monitor B850 is intended for use on adult, pediatric, and neonatal patients and on one patient at
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0731-2014·2014-01-22
GE Centricity PACS System Recalled for Potential Image Loss During Transfer
GE Healthcare is recalling Centricity PACS System versions 3.X and 4.X due to a potential loss of diagnostic images during transfers between servers.
Product
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 diagnostic and analysis tool for diagnostic images by trained healthcare professionals, including radiologists, physicians, technolo
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0620-2014·2014-01-08
GE Centricity Laboratory System Recall for Free-Text Data Loss
GE Healthcare is recalling 5 units of the Centricity Laboratory System because free-text data from instruments may be discarded if orders are not yet in the system.
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
1 state
HighFDA (Devices)·Z-0556-2014·2014-01-01
McKesson Radiology 12.0 PACS Recall for Missing Contrast Allergy Data
McKesson Information Solutions LLC is recalling McKesson Radiology 12.0 PACS because merging patient records may result in missing contrast allergy information.
Product
McKesson Radiology 12.0, Picture Archiving Communication System (PACSA).
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-2318-2013·2013-10-09
McKesson Horizon Medical Imaging System Recalled for Potential Image Loss
McKesson Information Solutions LLC is recalling Horizon Medical Imaging software versions 4.6.1 to 11.6. because a server configuration malfunction may cause the loss of digital medical images.
Product
McKesson Horizon Medical Imaging (HMI) Radiological Image Processing System, product versions 4.6.1 to 11.6., is a medical image and information management application intended to receive, transmit, store, retrieve, display, print and process digital medical images, digital medi
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-2301-2013·2013-10-09
Hologic Selenia Mammography System Software Recall for Image Deletion
Hologic is recalling 62 Selenia Full Field Digital Mammography Systems because software versions 5.0.x and 5.1.x may delete recent images when the hard drive reaches a 4,000-image threshold.
Product
Selenia Full Field Digital Mammography System with software versions 5.0.x and 5.1.x The Selenia Full Field Digital Mammography system generates digital mammography images that can be used for screening and diagnosis of breast cancer. The Selenia Full Field Digital Mammography
Category
Medical Device
Distribution
19 states
ModerateFDA (Devices)·Z-1859-2013·2013-08-07
Siemens syngo Dynamics Information System Recall for Data Loss Risk
Siemens is recalling syngo Dynamics Information System versions 9.5 and VA10A because images may not be saved when specific modality settings are used.
Product
syngo Dynamics Information System (sDIS) versions 9.5 and VA10A. The syngo¿ Dynamics system is intended for the acceptance, transfer, display, storage, archive, and manipulation of digital medical images, including quantification and reportgeneration. syngo¿ Dynamics is not
Category
Medical Device
Distribution
7 states
ModerateFDA (Devices)·Z-1585-2013·2013-07-03
GE Healthcare Recalls Centricity Laboratory System Software Due to Data Loss
GE Healthcare is recalling 9 units of Centricity Laboratory System software versions 3.3, 4.0, and 4.1 because a specific configuration can cause loss of free-text data in microbiology results.
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
6 states
ModerateFDA (Devices)·Z-1559-2013·2013-06-26
Hitachi Recalls Echelon and Oasis MR Imaging Systems Due to Software Error
Hitachi is recalling 45 Echelon, Echelon Oval, and Oasis MR imaging systems due to a software error that can cause image data loss during simultaneous scanning and processing.
Product
Echelon, Echelon Oval and Oasis MR imaging device systems; one unit per box. The Echelon, Echelon Oval and Oasis MR systems are imaging devices, and are intended to provide the physician with physiological and clinical information, obtained non-invasively and without the use
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1160-2013·2013-05-08
Hospira Recalls GemStar Infusion Pumps Due to Battery Data Loss
Hospira is recalling GemStar infusion pumps because low battery levels can corrupt data and cause an error that prevents the device from being used.
Product
GemStar Pump - Battery Product Usage: The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the hospital, or anywhere electronic infusion is required. The GemStar Pump can be powered by AC mains adaptor, rechargeable bat
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1159-2013·2013-05-08
Hospira Recalls GemStar Infusion Pumps Due to Battery Data Loss
Hospira Inc. is recalling GemStar infusion pumps because low battery levels can corrupt history logs and cause an error that prevents the device from being used.
Product
GemStar Pump - Battery Product Usage: The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the hospital, or anywhere electronic infusion is required. The GemStar Pump can be powered by AC mains adaptor, rechargeable b
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1112-2013·2013-04-24
Carefusion Recalls Alaris PC Unit 8015 Due to Bolus Programming Risk
Carefusion is recalling 4,090 Alaris PC unit model 8015 devices with software version 9.12 due to potential data loss risks during bolus programming.
Product
Alaris PC unit model 8015 with software version 9.12 Product Usage: The Alaris PC unit is the central programming, monitoring and power supply component for the Alaris System
Category
Medical Device
Distribution
Distributed nationwide