-
2026–2027 Grand Design Lineage recall: Incorrect Tire Pressure Information on Label/FMVSS 120
NHTSA
· Grand Design RV, LLC
-
2026 Grand Design Imagine recall: Incorrectly Secured 120V Outlet May Contact Wiring
NHTSA
· Grand Design RV, LLC
-
2021–2023 Ford F-150 and 1 more recall: Obstructed Rearview Camera Image/FMVSS 111
NHTSA
· Ford Motor Company
-
2025–2027 Newell P50 recall: Steer Axle Air Springs Base May Crack
NHTSA
· Newell Coach Corp.
-
2023–2025 Ford Mustang Mach E recall: Window Glass Trim Pieces May Detach
NHTSA
· Ford Motor Company
-
2025–2026 Foretravel Realm and 1 more recall: Unintended Brake Light Illumination/FMVSS 108
NHTSA
· Foretravel, Inc.
-
2027 Kenworth T280 and 11 more recall: Oil Contaminated Power Distribution Center/FMVSS 103
NHTSA
· PACCAR Incorporated
-
2024–2026 Entegra Anthem and 5 more recall: Unintended Brake Light Illumination/FMVSS 108
NHTSA
· Jayco, Inc.
-
2026 Entegra Anthem recall: Incorrect Tire Size on Certification Label
NHTSA
· Jayco, Inc.
-
2025 Frontrunner Frontrunner recall: Wheelchair Restraint Retractor May Not Lock
NHTSA
· Frontrunner Bus Group, Inc.
-
2019–2022 Mercedes-Benz A 220 and 27 more recall: Rollaway Risk from Door Switch Failure
NHTSA
· Mercedes-Benz USA, LLC
-
2027 Yamaha Boat Trailer recall: Trailer Tongue May Fail
NHTSA
· Midwest Industries, Inc.
-
2017–2026 Arboc Spirit OF Independence recall: Rear Spring Hanger May Detach
NHTSA
· ARBOC Specialty Vehicles, LLC
-
Peony Design Recalls Personalized Baby Bibs and Stroller Bags Due to Risk of Serious Injury or Death from Choking Hazard
CPSC
· Peony Design
-
CuddleCubs Creations Teething Toy Sets Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys…
CPSC
· YouRfocus
-
OeyUoc Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards…
CPSC
· Yuanxinxiang
-
Sviyatp Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards…
CPSC
· Sviyatp
-
Aojieni Silicone Recalls Sili Factory Pull String Teething Toys Due to Risk of Serious Injury or Death from Choking…
CPSC
· Aojieni Silicone
-
12-Drawer Fabric Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards…
CPSC
· Xuzhou Mingquanhe Household Co., Ltd., of Changzhou Jiaxuan Intelligence Furniture Co., Ltd.
-
EnHomee 9-Drawer Fabric Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards…
CPSC
· Xuzhou Mingquanhe Household Co., Ltd.
-
2020–2026 BMW S 1000 RR recall: Ignition Lock May Fail and Cause Engine Stall
NHTSA
· BMW of North America, LLC
-
2026–2027 Forest River OG Luxury Coach and 1 more recall: Printed Circuit Board May Overheat
NHTSA
· Forest River, Inc.
-
2027 Forest River Ibex and 6 more recall: Incorrect Water Tank Capacity on Label/FMVSS 110
NHTSA
· Forest River, Inc.
-
K&N Replacement Fuel Filter recall: Fuel Filter O-Ring May Disintegrate
NHTSA
· K&N Engineering, Inc. · Do not drive
-
ST AIA-Pack Testosterone, IN VITRO DIAGNOSTIC USE ONLY for the… recall
FDA
· Tosoh Bioscience Inc · Class II
-
Photera 600 3-D, phototherapy device recall
FDA
· Daavlin Distributing Company · Class II
-
Photera 600, phototherapy device recall
FDA
· Daavlin Distributing Company · Class II
-
Photera 400, phototherapy device recall
FDA
· Daavlin Distributing Company · Class II
-
The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000 recall
FDA
· Maquet Cardiovascular, LLC · Class II
-
Rio" II Product Name: Rio" II Nasal Pillows Interface Model recall
FDA
· 3B Medical, Inc. · Class II
-
Medtronic Bio-Medicus Adult Cannula Kit, Product Number/CFN 96530-115 recall
FDA
· Medtronic Perfusion Systems · Class II
-
Medtronic DLP One-Piece Pediatric Arterial Cannula… recall
FDA
· Medtronic Perfusion Systems · Class II
-
Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE… recall
FDA
· Medline Industries, LP · Class II
-
Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE… recall
FDA
· Medline Industries, LP · Class II
-
Papablic Replacement Brush Heads recall
FDA
· Papablic Inc · Class II
-
Papablic Replacement Brush Heads recall
FDA
· Papablic Inc · Class II
-
Orthofix MINIRAIL, ARTICULATED, FIXATOR, VERTICAL AXIS recall
FDA
· Orthofix U.S. LLC · Class II
-
Orthofix ARTICULATED MINIRAIL FIXATOR HORIZONTAL AXIS recall
FDA
· Orthofix U.S. LLC · Class II
-
Orthofix MINIRAIL, SHORT, LENGTHENER recall
FDA
· Orthofix U.S. LLC · Class II
-
Orthofix MINIRAIL, STANDARD LENGTHENER Model recall
FDA
· Orthofix U.S. LLC · Class II
-
Optima XR240amx, Mobile Digital Radiographic System recall
FDA
· GE Medical Systems, LLC · Class II
-
Optima XR220amx, Mobile Digital-Ready Radiographic System recall
FDA
· GE Medical Systems, LLC · Class II
-
Optima XR200amx, Mobile Digital-Ready Radiographic System recall
FDA
· GE Medical Systems, LLC · Class II
-
Rapid Refill Continuous Injection System, UPN M00566001 recall
FDA
· Boston Scientific Corporation · Class II
-
ICU Medical Plum Solo Precision IV Pump, v1.0.3, Item Number 400010401 recall
FDA
· ICU Medical, Inc. · Class II
-
ICU Medical Plum Duo Infusion Pump, v1.2.3: 1) Item Number 400020401 and… recall
FDA
· ICU Medical, Inc. · Class II
-
da Vinci SP Instrument Arm Drape, SP, 1-PACK, Part Number: 430013-13… recall
FDA
· Intuitive Surgical, Inc. · Class II
-
Olympus Glass Body for 194 Ellik Evacuator recall
FDA
· Olympus Corporation of the Americas · Class II
-
Olympus Ellik Evacuator Includes Glass Body… recall
FDA
· Olympus Corporation of the Americas · Class II
-
Olympus Toomey Evacuator 50cc with Adaptor recall
FDA
· Olympus Corporation of the Americas · Class II
-
Olympus Toomey Evacuator 30cc with Adaptor recall
FDA
· Olympus Corporation of the Americas · Class II
-
Bone Marrow Tray recall
FDA
· Argon Medical Devices, Inc · Class I
-
Arterial Line Kit 20ga x 6 recall
FDA
· Argon Medical Devices, Inc · Class I
-
T-Lok Bone Marrow Tray recall
FDA
· Argon Medical Devices, Inc · Class I
-
General Biospy Tray recall
FDA
· Argon Medical Devices, Inc · Class I
-
One-Piece Introducer Tray recall
FDA
· Argon Medical Devices, Inc · Class I
-
Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode 5F recall
FDA
· Argon Medical Devices, Inc · Class I
-
ABIOMED Intro Kit, 14Fr x 13 and 25 cm, PKGD, JP… recall
FDA
· Abiomed, Inc. · Class I
-
ABIOMED Insertion Kit, Pkgd, JP, Pump Set Code 0052-0011-JP recall
FDA
· Abiomed, Inc. · Class I
-
ABIOMED Impella CP Set, Pump Set Code 0048-0044 recall
FDA
· Abiomed, Inc. · Class I