-
Cinacalcet Hydrochloride Tablets, 30 mg, 30 Tablets per bottle, Rx Only… recall
FDA
· Cipla USA, Inc. · Class II
-
Morphine Sulfate Oral Solution 100 mg / 5 mL (20 mg* / mL), 30 mL… recall
FDA
· Winder Laboratories, LLC · Class III
-
Nebivolol Tablets, 20 mg, 90 Tablets, Rx Only… recall
FDA
· Glenmark Pharmaceuticals Inc., USA · Class III
-
Tropicamide 1%/Cyclopentolate 1%/Phenylephrine 2.5%/Ketorolac 0.5% Topical… recall
FDA
· Fagron Compounding Services · Class II
-
Ganirelix Acetate Injection, 250 mcg/0.5mL… recall
FDA
· Lupin Pharmaceuticals Inc. · Class II
-
Varenicline Tablets, 1mg, 56 Tablets, Rx only, Distributor: Dr recall
FDA
· Dr. Reddy's Laboratories, Inc. · Class III
-
Lanthanum Carbonate chewable tablets, 1000mg*… recall
FDA
· Cipla USA, Inc. · Class II
-
Lanthanum Carbonate chewable tablets, 1000mg*… recall
FDA
· Cipla USA, Inc. · Class II
-
2021–2025 Chrysler Pacifica and 2 more recall: Wheelchair Restraint Retractor May Not Lock
NHTSA
· Vantage Mobility
-
2023 Chevrolet Express 2500 and 12 more recall: Wheelchair Restraint Retractor May Not Lock
NHTSA
· Rollx Vans
-
2024 Autocar E-Actt recall: Improperly Secured Battery Cable Connections
NHTSA
· Autocar, LLC
-
2024–2025 KIA Sportage and 1 more recall: Blank Instrument Panel Screen/FMVSS 101
NHTSA
· Kia America, Inc.
-
2025–2026 Suzuki DR-Z400S and 1 more recall: Incorrectly Tightened Reservoir Tank Cap Fixing Screws/FMVSS 122
NHTSA
· Suzuki Motor USA, LLC
-
2024–2025 Toyota Highlander and 1 more recall: Incorrectly Installed Third Row Seat Belt Anchor
NHTSA
· Toyota Motor Engineering & Manufacturing
-
2014–2015 BMW 228I and 6 more recall: Air Bag Inflators May Rupture
NHTSA
· BMW of North America, LLC
-
Bell Scout AIR Helmet recall: Helmets May Not Adequately Protect User/FMVSS 218
NHTSA
· Bell Sports, Inc.
-
2025 Gillig LOW Floor recall: Wheelchair Restraint Retractor May Not Lock
NHTSA
· Gillig, LLC
-
2025–2026 Toyota Camry Hybrid and 1 more recall: Inverter May Lose Connection and Cause a Loss of Drive Power
NHTSA
· Toyota Motor Engineering & Manufacturing
-
2013 Gillig LOW Floor recall: Emergency Exit Window Latch May Fail/FMVSS 217
NHTSA
· Gillig, LLC
-
2010–2016 Mack Granite (GU) recall: Rear Brakes May Overheat
NHTSA
· Mack Trucks, Inc.
-
2026 Ford F-250 SD and 1 more recall: Right Rear Axle Shaft May Fail
NHTSA
· Ford Motor Company
-
2025 Mercedes-Benz AMG E 53 4MATIC+ Wagon recall: Loss of Drive Power from Damaged Wiring Harness
NHTSA
· Mercedes-Benz USA, LLC
-
2025–2026 Mercedes-Benz GLE 350 4MATIC recall: Incorrect Seat Belt Installed/FMVSS 208, 209
NHTSA
· Mercedes-Benz USA, LLC
-
2022–2026 Ford F-150 Lightning BEV and 2 more recall: Vehicle Rollaway Risk/FMVSS 114
NHTSA
· Ford Motor Company
-
2025–2026 Ford Escape and 1 more recall: Seat Belt Retractors Not Secured Properly
NHTSA
· Ford Motor Company
-
2025 Diamond Coach VIP recall: Wheelchair Restraint Retractor May Not Lock
NHTSA
· Diamond Coach Corporation
-
2022–2025 Ford E-Transit recall: Loss of Drive Power from Disengaged Axle Shaft
NHTSA
· Ford Motor Company
-
Luyuan Recalls Youth ATVs Due to Risk of Serious Injury or Death from Crash Hazard; Violate Mandatory Standard for All-Terrain Vehicles
CPSC
· Luyuan
-
Sanven Technology Recalls Vevor Ice Crushers Due to Fire Hazard
CPSC
· Sanven Technology
-
YCXXKJ Baby Bath Seats Recalled Due to Risk of Serious Injury or Death to Children from Drowning…
CPSC
· BenTalk
-
Sanven Technology Recalls VEVOR Steamers Due to Risk of Serious Injury from Burn Hazard
CPSC
· Sanven Technology
-
Uuoeebb Infant Walkers Recalled Due to Risk of Serious Injury or Death from Fall and Entrapment Hazards…
CPSC
· BaoD
-
SKCAIHT Children's Costumes Recalled Due to Risk of Injury from Phthalate Exposure; Violates Federal Phthalates Ban…
CPSC
· SKCAIHT Direct
-
Primark Recalls Little Bear 2-Pack Soother Clips Due to Choking and Laceration Hazards
CPSC
· Primark
-
TREK Recalls Electric Bicycles Due to Fall or Crash Hazard
CPSC
· Trek
-
2016–2020 Acura ILX recall: Reduced Brake Function
NHTSA
· Honda (American Honda Motor Co.)
-
2025 Honda Cr-V Fuel Cell EV recall: Loss of Drive Power/FMVSS 305
NHTSA
· Honda (American Honda Motor Co.)
-
2025–2026 BMW X3 recall: Unintended Steering Wheel Movement
NHTSA
· BMW of North America, LLC
-
2024–2026 GMC Canyon recall: Passenger Air Bag May Deploy Improperly/FMVSS 208
NHTSA
· General Motors, LLC
-
Q Straint Qrt-Max recall: Wheelchair Restraint Retractor May Not Lock
NHTSA
· Lippert
-
Reagent Kits/ containing flow cells, components of NextSeq 550Dx… recall
FDA
· Illumina, Inc. · Class II
-
Lumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841 recall
FDA
· Philips Ultrasound, Inc · Class II
-
CT 5300; Software Version Number: 4.5, 5.0, 5.1 recall
FDA
· Philips North America Llc · Class II
-
Incisive CT recall
FDA
· Philips North America Llc · Class II
-
Hemochron Activated Clotting Time Low-Range Test Cuvette recall
FDA
· Accriva Diagnostics, Inc. · Class II
-
MAMMOMAT Fusion recall
FDA
· Siemens Medical Solutions USA, Inc · Class II
-
MAMMOMAT Inspiration recall
FDA
· Siemens Medical Solutions USA, Inc · Class II
-
MAMMOMAT Revelation recall
FDA
· Siemens Medical Solutions USA, Inc · Class II
-
KWIK-STIK, Quality control kit for culture media… recall
FDA
· Microbiologics Inc · Class II
-
Olympus OER-Mini recall
FDA
· Aizu Olympus Co., Ltd. · Class II
-
Olympus OER-Pro recall
FDA
· Aizu Olympus Co., Ltd. · Class II
-
Olympus OER-Elite recall
FDA
· Aizu Olympus Co., Ltd. · Class II
-
Phantom Fibula Nail, 2.8mm x 130mm, Right, Ti, Fibula Nail recall
FDA
· Paragon 28, Inc. · Class II
-
IntelliVue Patient Monitor MX850. Product Number: 866470 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX800. Product Number: 865240 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX750. Product Number: 866471 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX700. Product Number: 865241 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX600. Product Number: 865242 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX550. Product Number: 866066 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX500. Product Number: 866064 recall
FDA
· Philips North America Llc · Class II