Hazard

Incorrect Display recalls

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

What the numbers show

Total: 17
Critical: 0
Severe: 0
Most recent: 2026-05-06

Of the 17 incorrect display 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 incorrect display 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.

1–17 of 17

ModerateFDA (Devices)·Z-1964-2026·2026-05-06
Philips MR 7700 MR Elastography device stiffness value error recall
Philips is recalling certain MR 7700 devices with MR Elastography due to potential stiffness value errors when specific image reconstruction parameters are used, which may cause voxel size settings to display incorrectly.
Product
Philips MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782120. 2. Model Number (REF): 782153.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0594-2026·2025-12-03
Diabetes clinic software recalled over incorrect sensor glucose graph data
Medtronic MiniMed is recalling 12,126 CareLink Clinic installations because a software error displays incorrect data on the 24-hour sensor glucose overview graph.
Product
CareLink Clinic, REF: MMT-7350
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1599-2024·2024-05-01
ACUSON Juniper ultrasound systems display incorrect cardiac measurements
Siemens ACUSON Juniper ultrasound systems may display the wrong cardiac measurement value when configured to show minimum or maximum values, potentially leading to misdiagnosis.
Product
ACUSON Juniper Diagnostic Ultrasound System, REF: 11335791, and ACUSON Juniper Select Diagnostic Ultrasound System, REF: 11653093, running software version VA10x with DICOM SR Cardiac option, from VB10A to VB10G, VB11A, VB11B, VB30B and VB30C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1098-2021·2021-02-17
Roche 9180 Electrolyte Analyzer Recalled for Incorrect Calcium Display Arrows
Roche Diagnostics is recalling 1,214 units of the 9180 Electrolyte Analyzer because the device may display incorrect arrow directions for ionized calcium results when configured in mg/dL, potentially leading to misinterpretation.
Product
9180 Electrolyte Analyzer - Product Usage: intended to be used for the measurement of sodium, potassium, chloride, ionized calcium and lithium in the whole blood, serum or plasma, urine, dialysate solutions, or QC materials. catalog number 03157334001 . in vitro diagnostic use.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1349-2020·2020-03-04
Randox RX Daytona Plus Clinical Chemistry Analyzer Software Recall
Randox Laboratories is recalling RX Daytona Plus clinical chemistry analyzers to fix software issues causing incorrect sample ordering and quality control flags.
Product
RX Daytona Plus (with ISE/without ISE); Models Nos. RX4040 (w/ISE) and RX4041 (without ISE) - Product Usage: A fully automated, random access, clinical chemistry analyzer complete with dedicated analyzer software. For use in clinical laboratories.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1330-2020·2020-02-26
Mindray DP-30 Ultrasound Systems Recalled for Incorrect Needle-Guide Display
Mindray is recalling 53 DP-30 ultrasound systems and 18 USB drives because the devices display an incorrect needle-guide bracket when used with a specific transducer.
Product
DP-30 Digital Ultrasonic Diagnostic Imaging System, Part No. 1155E-PA00004 - Product Usage: The Digital Ultrasonic Diagnostic Imaging System is applicable for adults, pregnant women, pediatric patients and neonates. It is intended for use in fetal, abdominal, pediatric, small org
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0826-2020·2020-01-29
Acclarent Recalls TruDi NAV Suction Instruments Due to Calibration Issues
Acclarent, Inc. is recalling three lots of TruDi NAV Suction Instruments because calibration issues cause incorrect tip orientation displays.
Product
TruDi NAV Suction, TDNS090Z, 90 Degree Tip Angle, (01) 10705031245891
Category
Medical Device
Distribution
6 states
ModerateFDA (Devices)·Z-0824-2020·2020-01-29
Acclarent Recalls TruDi NAV Suction Instruments Due to Calibration Issues
Acclarent, Inc. is recalling TruDi NAV Suction Instruments because calibration issues cause incorrect tip orientation displays.
Product
TruDi NAV Suction, TDNS000Z, 0 Degree Tip Angle, (01)10705031245877
Category
Medical Device
Distribution
6 states
ModerateFDA (Devices)·Z-0686-2020·2019-12-25
CVS Health At Home A1C Test Kit Recalled for Software Bug
Polymer Technology Systems is recalling CVS Health At Home A1C Test Kits due to a software bug that may display incorrect numerical values for extreme results.
Product
CVS Health At Home A1C Test Kit, Software Version Revision D, REF Number 3059
Category
Medical Device
Distribution
18 states
HighFDA (Devices)·Z-0973-2019·2019-03-13
Stryker Reprocessed Arthroscopic Shavers Recalled for Display and Function Errors
Stryker is recalling 14,265 reprocessed arthroscopic shavers that may display incorrect settings or error messages, preventing proper use during surgery.
Product
Stryker Sustainability Solutions (SSS) reprocessed Arthroscopic Shavers Arthroscopic shavers can be used to abrade, cut and excise tissue and bone; remove loose fragments; and, shave away debris in arthroscopic surgeries, as well as surgeries of the jaw and sinuses. Intended
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2335-2018·2018-07-11
St Jude Medical Recalls Merlin PCS Programmer Software for ICM Battery Display Error
St Jude Medical is recalling Merlin PCS Programmer Software to address an incorrect low battery indicator on Confirm Rx ICM devices caused by supply chain temperature exposure.
Product
Merlin PCS Programmer Software: 3330 The Merlin PCS programmer (model 3650) is a portable, external device used to support the implanted device, and for this recall the software that resides on the programmer (software model 3330) is the method of delivery of the new firmware.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1292-2018·2018-04-11
GE Healthcare Recalls Monica Novii Wireless Patch System Due to Signal Swap Risk
GE Healthcare is recalling 1,742 units of the Monica Novii Wireless Patch System because incorrectly reconnected cables may cause fetal and maternal heart rate signals to be displayed swapped.
Product
Uterine Electromyographic Monitor - Monica Novii Wireless Patch System Product Usage: The Novii Interface is an accessory to the Novii Pod which provides a means of interfacing the wireless output of the Novii Pod to the transducer inputs of a CTG Fetal monitor via three cabl
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1212-2017·2017-02-22
Siemens ARTISTE MV System Recalled for Collimator and Weld Defects
Siemens is recalling 194 ARTISTE MV radiation therapy systems due to incorrect collimator position displays and improper weld seams.
Product
ARTISTE MV System, medical charged-particle radiation therapy system Product Usage: The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer.
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1214-2017·2017-02-22
Siemens Recalls ONCOR Radiation Therapy Systems Due to Collimator and Weld Defects
Siemens is recalling 194 ONCOR radiation therapy systems in the US due to incorrect collimator position displays and improper weld seams.
Product
ONCOR Impression, ONCOR Impression plus, and ONCOR Expression Medical charged-particle radiation therapy system Product Usage: The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cance
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2440-2015·2015-09-02
Brainlab ExacTrac 6.0 Patient Positioning System Recalled for Display Error
Brainlab AG is recalling ExacTrac 6.0.x software due to a potential display error in Digitally Reconstructed Radiographs used for x-ray correction.
Product
ExacTrac 6.0.x Patient Positioning System, Radiation therapy. Intended to be used to place patients at an accurately defined point within the treatment beam of a medical accelerator for stereotactic radiosurgery or radiotherapy procedures.
Category
Medical Device
Distribution
32 states
HighFDA (Devices)·Z-1972-2015·2015-07-08
Siemens Recalls Syngo Imaging Software Due to Display and Measurement Errors
Siemens is recalling Syngo Imaging software versions V30 and V31 because safety issues may occur involving monitor assignment order and incorrect display and measurements for images with non-square pixel size.
Product
SYNGO IMAGING (VERSION V30 and V31); Syngo Imaging is a Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images, including digital mammography images.
Category
Medical Device
Distribution
2 states
ModerateFDA (Devices)·Z-1067-2013·2013-04-17
Toshiba Aquilion 32/64 CT Systems Recalled for Software Display Error
Toshiba American Medical Systems is recalling 23 Aquilion 32/64 CT scanners due to a software issue that may cause incorrect Dose Length Product values to display.
Product
TSX-IOI: AQUILION 32/64; System, X-Ray, Tomography, Computed. Designed to produce cross-sectional images of a human body.
Category
Medical Device
Distribution
Distributed nationwide