-
Delta Gas Ball Valves Recalled Due to Fire and Burn Hazards; Manufactured by Masco Canada
CPSC
· Masco Canada Limited
-
Yamaha Corporation of America Recalls Power Adaptors for Digital Pianos and Music Workstations Due to Burn and Fire Hazards
CPSC
· Yamaha
-
Igloo Expands Recall of 90 Qt. Rolling Coolers Due to Fingertip Amputation and Crushing Hazards; Total Recalled Now Nearly 1.2 Million
CPSC
· Igloo
-
Xylolin Peg Doll Toy Sets Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violation of Federal Regulations for Toys…
CPSC
· Babywants
-
Sanven Technology Recalls Vevor Cable Railing Kits Due to Entrapment Hazard
CPSC
· Sanven Technology
-
DEMDACO Recalls Maril Brand Scented Candles Due to Laceration and Fire Hazards
CPSC
· Demdaco
-
2022–2025 Chrysler Pacifica and 1 more recall: Improperly Sealed Side Curtain Air Bag/FMVSS 226
NHTSA
· Chrysler (FCA US, LLC)
-
2025–2026 Thor Motor Coach Outlaw recall: Removable Steps May Detach While In Use
NHTSA
· Thor Motor Coach
-
2024 Aston Martin Valkyrie recall: Fuse Box Attached with Incorrect Length Screws
NHTSA
· Aston Martin The Americas
-
2025 Chevrolet Express and 1 more recall: Improperly Welded Head Restraint
NHTSA
· General Motors, LLC
-
2019–2024 RAM 1500 recall: Improperly Connected Air Bag/FMVSS 208
NHTSA
· Chrysler (FCA US, LLC)
-
2025 RAM 2500 and 1 more recall: Inaccurate Gear Selection Display/FMVSS 101
NHTSA
· Chrysler (FCA US, LLC)
-
2022–2025 Volvo C40BEV and 11 more recall: Rearview Camera Image May Not Display/FMVSS 111
NHTSA
· Volvo Car USA, LLC
-
Mopar AIR BAG recall: Improperly Sealed Side Curtain Air Bag/FMVSS 226
NHTSA
· Chrysler (FCA US, LLC)
-
Powered Laser Surgical Instrument Product Name: SOLTIVE Pro SuperPulsed… recall
FDA
· Olympus Corporation of the Americas · Class II
-
Medline procedure kits, labeled as: HAND recall
FDA
· Medline Industries, LP · Class II
-
Medline procedure kits, labeled as: OL OCULAR recall
FDA
· Medline Industries, LP · Class II
-
Medline procedure kits, labeled as: REDDY JOINT BATH recall
FDA
· Medline Industries, LP · Class II
-
Medline procedure kits, labeled as: 1) WOUND CARE TRAY recall
FDA
· Medline Industries, LP · Class II
-
Medline procedure kits, labeled as: PLASTICS SUTURE TRAY recall
FDA
· Medline Industries, LP · Class II
-
Medline procedure kits, labeled as: 1) STERILE PREP KIT recall
FDA
· Medline Industries, LP · Class II
-
Medline procedure kits, labeled as: NON STERILE I&D KIT recall
FDA
· Medline Industries, LP · Class II
-
Medline procedure kits, labeled as: T AND A PACK -LF recall
FDA
· Medline Industries, LP · Class II
-
Medline Sterile 0.9% Normal Saline, USP, 100mL recall
FDA
· Medline Industries, LP · Class II
-
Medline Sterile Water, USP, 100mL recall
FDA
· Medline Industries, LP · Class II
-
Enhanced Verify Evaluation Handset (CFN HH90130FA) recall
FDA
· Medtronic Neuromodulation · Class II
-
myQA iON recall
FDA
· IBA Dosimetry GmbH · Class II
-
Tibial Augment recall
FDA
· Waldemar Link GmbH & Co. KG (Mfg Site) · Class II
-
L-Shaped Femoral Augment recall
FDA
· Waldemar Link GmbH & Co. KG (Mfg Site) · Class II
-
Posterior Femoral Augment recall
FDA
· Waldemar Link GmbH & Co. KG (Mfg Site) · Class II
-
Distal Femoral Augment recall
FDA
· Waldemar Link GmbH & Co. KG (Mfg Site) · Class II
-
Quantum Informatics - VISION / LIVE VUE Product Name: Monitor… recall
FDA
· Spectrum Medical Ltd. · Class II
-
Quantum Informatics - VIPER Product Name: Monitor, Physiological… recall
FDA
· Spectrum Medical Ltd. · Class II
-
Automated External Defibrillators, Model DDU-2200… recall
FDA
· Defibtech, LLC · Class II
-
Automated External Defibrillators, Model DDU-2450… recall
FDA
· Defibtech, LLC · Class II
-
Automated External Defibrillators, Model DDU-2300… recall
FDA
· Defibtech, LLC · Class II
-
Automated External Defibrillators, Model DDU-2200… recall
FDA
· Defibtech, LLC · Class II
-
Semi-Automated External Defibrillators recall
FDA
· Defibtech, LLC · Class II
-
IceSeed 1.5 CX NEEDLE OUS, Cryoablation Needle recall
FDA
· Boston Scientific Corporation · Class II
-
IceSeed 1.5 CX NEEDLE US, Cryoablation Needle recall
FDA
· Boston Scientific Corporation · Class II
-
IceSeed 1.5 CX S NEEDLE OUS, Cryoablation Needle recall
FDA
· Boston Scientific Corporation · Class II
-
IceSeed 1.5 CX S NEEDLE US, Cryoablation Needle recall
FDA
· Boston Scientific Corporation · Class II
-
epoc BGEM Crea Test Card (25 pk) for the epoc Blood Analysis System recall
FDA
· Siemens Healthcare Diagnostics, Inc. · Class II
-
epoc BGEM BUN Test Card (25 pk) for the epoc Blood Analysis System recall
FDA
· Siemens Healthcare Diagnostics, Inc. · Class II
-
HistoCore PELORIS 3, Model recall
FDA
· Leica Biosystems Melbourne Pty Ltd · Class II
-
3.0 Liter Disposable Set (4 sets/case) recall
FDA
· Belmont Instrument LLC · Class II
-
Straight Inflow/Bifurcated Outflow Line Kit recall
FDA
· Belmont Instrument LLC · Class II
-
Straight Inflow/Outflow Patient Line Kit recall
FDA
· Belmont Instrument LLC · Class II
-
Hyperthermia Pump Procedure Kit recall
FDA
· Belmont Instrument LLC · Class II
-
Stratus CS Acute Care cTNI TestPak.IVD test for cardiac troponin I in… recall
FDA
· Siemens Healthcare Diagnostics, Inc. · Class II
-
DxC 500 AU Clinical Chemistry Analyzer recall
FDA
· Beckman Coulter, Inc. · Class II
-
The Trimble RTS873 robotic total station is a solution designed for… recall
FDA
· Trimble Ab · Class II
-
GE Healthcare CARESTATION 750c A2, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare CARESTATION 750c A1, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare CARESTATION 750 A2, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare CARESTATION 750 A1, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare Carestation 650c A1, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare CARESTATION 650C A2, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare CARESTATION 650C A1, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare Carestation 650 A1, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I