Vehicles & Parts
HIGH
NHTSA
Mazda CX-70 2025 Recalled for Inverter Software Error Prompting EV Drive Power Loss
Mazda
Loss of
immediate action Recalls
2,756 recalls tagged with “immediate action”.
Vehicles & Parts
HIGH
NHTSA
Mazda CX-90 Recalled for Dash ESU Software Issue Affecting 2024-2025 CX-90 and 2025 CX-70 (Recall 12
Mazda
An ESU
Health & Personal Care
HIGH
FDA DEVICE
CorNeat Vision EverPatch 1036295 Recall for Labeling Update in 2024
Retroactive; Due to complaints, labeling correction for permanent tissue-integrating surgical matrices to include prevention and management of would dehiscence.
CorNeat Vision
Retroactive; Due
Health & Personal Care
HIGH
FDA DEVICE
Olympus Cystoscope Outer Sheath Recalled Over Laser Incompatibility
Product being removed due to incompatibility when used in conjunction with a GreenLight Laser for BPH therapy which could damage the tip of the device.
Olympus Corporation of the Americas
Product being
Health & Personal Care
HIGH
FDA DEVICE
Intuitive Surgical Recalls da Vinci 5 Console Motor Connector Due to High Hazard
Intuitive Surgical
Surgical system
Health & Personal Care
HIGH
FDA DEVICE
Omnia Medical TiBrid Stand Alone Fusion Device Recalled for Field Instrument Failure
Failure of fusion system instruments in the field.
Omnia Medical
Failure of
Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalls Electrosurgical Knife Over Burning Risk
A deterioration of the cutting knife, including overheating and burning, can contribute to tip breakage during use.
Olympus Corporation of the Americas
A deterioration
Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalls Electrosurgical Knife Over Burn Hazard
A deterioration of the cutting knife, including overheating and burning, can contribute to tip breakage during use.
Olympus Corporation of the Americas
A deterioration
Health & Personal Care
HIGH
FDA DEVICE
NOXBOX LTD Recalls NOxBOXi Nitric Oxide Delivery System in US for Pump Failure
Replacement of the internal Sample Pump due to high failure rates.
NOXBOX
Replacement of
Health & Personal Care
HIGH
FDA DEVICE
Surepulse Medical Recalls Newborn Heart Rate Monitor Component Due to Labeling Error
Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.
SUREPULSE MEDICAL
Retroactively reported;
Health & Personal Care
HIGH
FDA DEVICE
Surepulse Medical Issues Recall for Newborn Heart Rate Monitor Component
Surepulse Medical recalled the VS Cap Small component of its newborn heart rate monitor on January 20, 2023. The recall stems from incorrect sizing information provided on the product label. This defect poses a significant risk to patient safety.
SUREPULSE MEDICAL
Retroactively reported;
Health & Personal Care
HIGH
FDA DEVICE
Surepulse Medical Recalls Heart Rate Monitor Component Over Sizing Error
Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.
SUREPULSE MEDICAL
Retroactively reported;
Health & Personal Care
HIGH
FDA DEVICE
Surepulse Heart Rate Monitor Cap Recalled for Sizing Error
Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.
SUREPULSE MEDICAL
Retroactively reported;
Health & Personal Care
HIGH
FDA DEVICE
Surepulse Medical Recalls Heart Rate Monitor Component Over Sizing Error
Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.
SUREPULSE MEDICAL
Retroactively reported;
Health & Personal Care
HIGH
FDA DEVICE
Foundation Medicine FoundationOne CDx Recalled for Missing Companion Diagnostic Claims Page
Reports were sent to customers without the companion diagnostic (CDx) Claims Page. Claims pages were distributed via amended reports within 7 days of the issue occurrence.
Foundation Medicine
Reports were
Health & Personal Care
HIGH
FDA DEVICE
Foundation Medicine FoundationOne Liquid CDx Recall 2022 Reminds Clinicians to Check CDx Pages (18 U
Reports were sent to customers without the companion diagnostic (CDx) Claims Page. Claims pages were distributed via amended reports within 7 days of the issue occurrence.
Foundation Medicine
Reports were
Tag Statistics
Total Recalls
2,756