Hazard
30 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 30 display defect 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.
Which agencies issued them
Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all display defect 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.
Trividia Health is recalling 601 Good Neighbor Pharmacy TRUE METRIX blood glucose meters over a display defect that can cause glucose values to be misread.
ACUSON Maple ultrasound systems display the last cardiac measurement value instead of the configured minimum or maximum, potentially causing patient misdiagnosis during cardiac assessment.
The TactiFlex Ablation Catheter is not correctly recognized by the EnSiteX EP System, which displays it as a different model, prevents certain features from appearing, and may show an inverted image.
Philips is recalling Incisive CT scanners due to nine software defects including image artifacts, incorrect orientation labels, display failures, and positioning errors that could lead to misdiagnosis or need for rescans. No illnesses have been reported.
Baxter Healthcare is recalling the Welch Allyn Connex Spot Monitor due to improper placement of copper tape on the back of the liquid-crystal display. The device was distributed in California.
Rolls-Royce is recalling 2019-2022 Phantom vehicles because the central display may not raise correctly, partially blocking the rearview camera image.
CareFusion 303, Inc. is recalling Alaris Syringe Module Model 8110 units because the LED display may show dim segments, potentially affecting the visibility of infusion or patient monitoring values.
CareFusion 303, Inc. is recalling Alaris EtCO2 Module Model 8300 units because LED display segments may appear dim, potentially affecting the visibility of infusion or patient monitoring values.
CareFusion 303, Inc. is recalling Alaris PCA Module Model 8120 units because the LED display may show dim segments, potentially affecting the visibility of infusion or patient monitoring values.
CareFusion 303, Inc. is recalling Alaris Pump Module Model 8100 units because LED display segments may appear dim, potentially affecting the visibility of infusion or patient monitoring values.
CareFusion 303, Inc. is recalling Alaris SpO2 Modules because the LED display may have dim segments, potentially affecting the visibility of infusion or patient monitoring values.
Eizo Corporation is recalling 1,466 RadiForce RX360 medical monitors because a marble pattern may infrequently appear on the display under certain conditions.
Eizo Corporation is recalling 96 RadiForce GX560 monochrome LCD monitors because a marble pattern may infrequently appear on the screen under certain conditions.
SVO Group is recalling 2017-2018 Ford E-350 and E-450 shuttle buses because backup camera images may reverse, increasing crash risk.
Mickey Truck Bodies is recalling 2017-2018 Ford F-750 vehicles because back-up camera monitors may revert to factory settings, causing the image to reverse and increasing crash risk.
LGE Coachworks is recalling 2018-2019 Ford and Freightliner vans because back-up camera displays may revert to factory settings, reversing the image and increasing crash risk.
ITI is recalling 2018-2019 HINO 268 and 338 vehicles because backup camera displays may revert to factory settings, causing reversed images and increasing crash risk.
VCI Emergency Vehicle Specialists is recalling ambulances where backup camera monitors may revert to factory settings, causing reversed images and increasing crash risk.
PL Custom is recalling 2017-2019 Type I and III ambulances because backup camera monitors may revert to factory settings, reversing the image and increasing crash risk.
Halcore Group is recalling 2016-2019 AEV TraumaHawk ambulances because backup camera displays may revert to factory settings, causing the image to reverse and increasing crash risk.
Halcore Group is recalling 2016-2019 Horton ambulances because backup camera displays may revert to factory settings, causing the image to reverse and increasing crash risk.
VT Hackney is recalling 2018-2019 Beverage Trailers because back-up camera displays may revert to factory settings, causing the image to reverse and increasing crash risk.
REV Ambulance Group is recalling 2018-2019 Road Rescue Ultramedic vehicles because backup camera displays may revert to factory settings, causing the image to reverse.
Forest River is recalling 2018-2019 motorhomes, work trucks, and shuttle buses because backup camera images may display in reverse, increasing crash risk.
Spartan Motors is recalling 2018-2019 Utilimaster Truck Body and Velocity vehicles because backup camera monitors may display reversed images, increasing crash risk.