Vehicles & Parts
HIGH
NHTSA
AUDI Q4 e-tron, ID.4 Recalled Over On-Board Charger Failure Potentially Cutting Drive Power (2025)
Audi
A loss
cpsc regulated Recalls
2,143 recalls tagged with “cpsc regulated”.
Vehicles & Parts
HIGH
NHTSA
Kia EV9 Recalled for Rear GDU Weld Flaw in 2025 Model Year
Kia America, Inc. (Kia) is recalling certain 2025 EV9 vehicles. The rear gear drive unit (GDU) motor shaft may have been improperly welded and become damaged, causing a loss of drive power.
Kia America, Inc.
A loss
Vehicles & Parts
HIGH
NHTSA
BMW 2025 X3 Recalled for Electrical Cable Overheating After Tightening Issue
BMW of North America, LLC (BMW) is recalling certain 2025 X3 30 xDrive vehicles. The connection between the positive battery cable and the starter-generator may have been improperly tightened and overheat.
BMW
An overheated
Health & Personal Care
HIGH
FDA DRUG
World Perfumes Inc. Recalled Iodo Blanco Iodides First Aid Antiseptic Over Leaking Containers (2025)
Defective Container: broken or leaking bottles.
World Perfumes
Defective Container:
Health & Personal Care
HIGH
FDA DEVICE
MEDITECH Expanse Lab Calculator Module Recalled for Input Error Risk in 2025
Entering multiple keys that trigger input simultaneously may remove data from first field of screens and/or questionnaires with more than one field.
Medical Information Technology
Entering multiple
Vehicles & Parts
HIGH
Vehicles & Parts
HIGH
NHTSA
Mazda CX-70 2025 Recalled for Inverter Software Error Prompting EV Drive Power Loss
Mazda
Loss of
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
Vehicles & Parts
HIGH
NHTSA
Mazda CX-70 Recall 2025 for Powertrain Control Module Software May Lose Drive Power
Mazda North American Operations (Mazda) is recalling certain 2024 CX-90 and 2025 CX-70 vehicles. The powertrain control module (PCM) and engine control modules (ECM) software may cause malfunction indicator lights to illuminate and a loss of drive power.
Mazda
Loss of
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 Fusion Device and Angled Screwdrivers Recalled for Field Instrument Failure (Z-
Failure of fusion system instruments in the field.
Omnia Medical
Failure of
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 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
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
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 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 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 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;