-
ESTRADIOL, 6 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln… recall
FDA
· Asteria Health) · Class II
-
Doxazosin Tablets, USP, 4 mg, 1000 tablets per bottle, Rx only… recall
FDA
· Unichem Pharmaceuticals USA Inc. · Class III
-
Pro Numb Tattoo Numbing Spray, For Sensitive Skin, 4% Lidocaine… recall
FDA
· Pro Numb Tattoo Numbing Spray LLC · Class II
-
Pro Numb Tattoo Numbing Spray, 5% Lidocaine… recall
FDA
· Pro Numb Tattoo Numbing Spray LLC · Class II
-
2025 Lexus LS Hybrid and 1 more recall: Loss of Drive Power from Transmission Damage
NHTSA
· Toyota Motor Engineering & Manufacturing
-
2025–2026 Prevost X3-45 Commuter recall: Improperly Installed Passenger Seat Anchors
NHTSA
· Prevost Car (US) Inc.
-
2022–2026 Ford Escape Phev and 1 more recall: High Voltage Battery May Short Circuit
NHTSA
· Ford Motor Company
-
2025 Ford Transit recall: Do Not Drive - Loss of Brake Function/FMVSS 105
NHTSA
· Ford Motor Company · Do not drive
-
2020–2023 Winnebago Navion and 1 more recall: Rear Roof Cap May Detach
NHTSA
· Winnebago Industries, Inc.
-
2024–2025 Blue ARC BA4L-800 recall: Gearbox May Bind and Cause Loss of Steering
NHTSA
· Shyft Group
-
2023–2025 Thomas Built Buses Saf-T-Liner EFX and 1 more recall: Heater Hose May Leak Hot Heating Coolant Inside Passenger Compartment
NHTSA
· Daimler Trucks North America, LLC
-
2023–2026 Thomas Built Buses Saf-T-Liner EFX and 1 more recall: Heater Hose May Leak Hot Heating Coolant Inside Passenger Compartment
NHTSA
· Daimler Trucks North America, LLC
-
2022 Cadillac Escalade and 5 more recall: Rear Wheel Lock Up from Transmission Control Valve Failure
NHTSA
· General Motors, LLC
-
Hyperax Volt RV 4x recall: Bike Carrier May Detach
NHTSA
· Couture Co Ltd
-
Watkins Manufacturing Recalls Hydromassage Rotary Jets in Highlife Collection Spas Due to Entanglement and Drowning Hazards
CPSC
· Watkins Manufacturing
-
Beloems Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation…
CPSC
· Beloems
-
CheerKid Baby Bath Seats Recalled Due to Risk of Serious Injury or Death to Children from Drowning…
CPSC
· Babibaby
-
Surveying Accessories Cheaper Recalls Board Games Due to Risk of Serious Injury or Death from Magnet Ingestion…
CPSC
· Surveying Accessories Cheaper
-
Fortemotus Direct Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation…
CPSC
· Fortemotus Direct US
-
SOOWERY 6-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards…
CPSC
· Soowery
-
LShome Photoelectric Smoke Detector Fire Alarms Recalled Due Failure to Warn During Fire Posing Serious Injury or Death Hazard…
CPSC
· Tianjinshihaoweixinshengjidiananzhuanggongcheng
-
2026–2027 International MV recall: Brakes May Fail to Activate with Adaptive Cruise Control
NHTSA
· International Motors, LLC
-
2020–2022 Chevrolet Silverado 1500 and 5 more recall: Rear Wheel Lock Up from Transmission Control Valve Failure
NHTSA
· General Motors, LLC
-
2024 Cadillac Lyriq recall: Rearview Camera May Fail
NHTSA
· General Motors, LLC
-
2024–2025 Nissan Rogue recall: Gears in the Electronic Throttle Body May Break
NHTSA
· Nissan North America, Inc.
-
2023–2025 Nissan Rogue recall: Engine Failure
NHTSA
· Nissan North America, Inc.
-
Molift Product Name: Molift 4-point sling bars (Accessory to mobile… recall
FDA
· Etac A/S · Class II
-
Molift Product Name: Molift 2-point sling bars (Accessory to mobile… recall
FDA
· Etac A/S · Class II
-
Molift Product Name: Molift Mover 300 Model recall
FDA
· Etac A/S · Class II
-
Molift Product Name: Molift Mover 205 Model recall
FDA
· Etac A/S · Class II
-
Lumipulse ¿-Amyloid Plasma Controls Model recall
FDA
· Fujirebio Diagnostics, Inc. · Class II
-
Lumipulse G ¿-Amyloid 1-42-N Plasma Calibrators Model recall
FDA
· Fujirebio Diagnostics, Inc. · Class II
-
Lumipulse G ¿-Amyloid 1-42-N Plasma Immunoreaction Cartridges Model recall
FDA
· Fujirebio Diagnostics, Inc. · Class II
-
Lumipulse pTau 217 Plasma Controls Model recall
FDA
· Fujirebio Diagnostics, Inc. · Class II
-
Lumipulse G pTau 217 Plasma Calibrators Model recall
FDA
· Fujirebio Diagnostics, Inc. · Class II
-
Lumipulse G pTau 217 Plasma Immunoreaction Cartridges Model recall
FDA
· Fujirebio Diagnostics, Inc. · Class II
-
Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio Model recall
FDA
· Fujirebio Diagnostics, Inc. · Class II
-
Bubble Sensor for 3/8" x 3/32" tubing recall
FDA
· Maquet Cardiopulmonary Gmbh · Class II
-
FDR Visionary Suite recall
FDA
· FUJIFILM Healthcare Americas Corporation · Class II
-
Nasal Jejunal Feeding Tube recall
FDA
· Wilson-Cook Medical Inc. · Class II
-
Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Disposable Triple Lumen Sphincterotome Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Disposable Triple Lumen Sphincterotome Product Name: Disposable Triple… recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Disposable Triple Lumen Sphincterotome Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Disposable Triple Lumen Sphincterotome Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Disposable Triple Lumen Sphincterotome Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Disposable Triple Lumen Sphincterotome Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Disposable Triple Lumen Sphincterotome Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
FDA
· Olympus Corporation of the Americas · Class II
-
Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
FDA
· Olympus Corporation of the Americas · Class II