Search by meaning, not just keywords: describe the product or the hazard and we find matching recalls even when the official notice uses different words. Brand names and model numbers work too.
Latest recalls
35,025 found- Use cautionVehicle
FORD BRONCO SPORT (2021) recall — Visibility
Ford recalls 2021 Bronco Sport vehicles with potentially unsecured moonroof glass that could detach and cause crashes or injuries. Affected owners should contact Ford for free glass inspection and replacement.
FordOct 15, 2021 - Use cautionVehicle
FORD EXPEDITION (2021) recall — Air Bags
Ford recalls 2021 Expedition vehicles with front door side impact sensors that may not deploy air bags during crashes, risking injury. Owners must have sensors replaced free by dealers.
FordOct 15, 2021 - Use cautionVehicle
FORD RANGER (2020) recall — Seat Belts
Ford is recalling 2020 Ranger vehicles with potentially misrouted front seat belts that may not restrain occupants during crashes. Owners should inspect seat belts and contact dealers for free replacements if needed.
FordOct 15, 2021 - Lower riskMedical device
Karl Storz Endoscopy recalls Karl Storz Udel Sterilization Tray Instructions for Use, Tray Part Number/Description: 39301ACTS/CAMERA TRAY (STERRAD,
Karl Storz recalls specific sterilization trays with outdated instructions that may affect sterilization effectiveness. Updated instructions now specify compatible endoscope sizes and exclude ethylene oxide as a sterilization method.
Karl StorzOct 15, 2021 - Lower riskMedical device
GE Healthcare, LLC recalls GE Centricity Universal Viewer Zero Footprint Client
GE Healthcare recalls Centricity Universal Viewer Zero Footprint Client versions with incomplete patient imaging study display. Affected units may need software update to prevent image display issues.
GE HealthcareOct 15, 2021 - Lower riskMedical device
Ortho-Clinical Diagnostics, Inc. recalls VITROS Immunodiagnostic Products Anti-HBc IgM Controls, Product Code 6801427 For use in monitoring the performance of
Ortho-Clinical Diagnostics recalls VITROS Anti-HBc IgM Controls (Lot 1690) due to possible delayed test results from incorrect troubleshooting. No safety risk but may affect lab results.
Ortho-Clinical DiagnosticsOct 15, 2021 - Lower riskMedical device
The Binding Site Group, Ltd. recalls Freelite Human Lambda Free Kit (for use on the SPAPLUS) REF LK018.S Freelite Human Lambda Free Kit (for use on the
The Binding Site Group recalls Freelite Human Lambda Free Kit (REF LK018.S) due to calibration issues that may cause inaccurate test results. Affected units include specific lot numbers and model numbers.
The Binding Site GroupOct 15, 2021 - UnratedMedical device
Medtronic Vascular, Inc. recalls Endurant II Stent Graft System REF/Description: ETBF2513C145EE STENT GRAFT ETBF2513C145EE ENDUR II BIF ETBF2820C166EE
Medtronic recalls Endurant II Stent Graft Systems with specific model numbers due to risk of spindle detaching during deployment, which could cause complications. Affected units include ETBF2513C145EE and other variants listed in the recall.
MedtronicOct 15, 2021 - Lower riskMedical device
Howmedica Osteonics Corp. recalls 28MM -4 LFIT V40 HEAD, Catalog Number 6260-9-122
Howmedica Osteonics recalls 28MM-4 LFIT V4:10 heads with catalog number 6260-9-122 due to potential Tyvek lid debonding from sealed packaging.
Howmedica OsteonicsOct 15, 2021 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Dimension Vista 500- In-vitro diagnostic device intended to duplicate manual analytical procedures such as pipetting,
Siemens Healthcare recalls Dimension Vista 500 diagnostic devices with incorrect HIL index settings that could lead to inaccurate test results. Affected units have specific serial numbers and software versions.
Siemens HealthcareOct 15, 2021 - Lower riskMeat & poultry
Evans Food Group Recalls Pork Products Imported Without Benefit of Inspection
USDA recalls 10,359 pounds of pork products imported without re-inspection. Consumers urged not to consume or discard items bearing USDA inspection number EST. 6030.
Evans Food GroupOct 14, 2021 - Use cautionVehicle
RAM 2500 (2021) recall — Electrical System
Chrysler recalls 2021 RAM 2500 trucks with electrical short risk causing fire. Park away from buildings until fixed by dealer. Contact FCA US at 1-800-853-1403.
FCA USOct 14, 2021 - Use cautionVehicle
JEEP GRAND CHEROKEE (2021) recall — Exterior Lighting
Certain 2021 Jeep Grand Cherokee L models may have difficulty activating high beams, risking reduced visibility and crashes. Dealers will reprogram free of charge.
JeepOct 14, 2021 - Lower riskMedical device
Cardiac Assist, Inc recalls SHIP KIT, PROCEDURE KIT, PROTEKDUO LS - DL31 for temporary Cardiopulmonary bypass. Including the following components:
Cardiac Assist recalls specific cardiac bypass kits due to incorrect expiration date labels on packaging. Affected kits may have safety risks if used without proper expiration verification.
Cardiac AssistOct 14, 2021 - Lower riskMedical device
FujiFilm Healthcare Americas Corporation recalls Arietta 65 Ultrasound Software Versions: V1.0 through V4.0.0
FujiFilm recalls Arietta 65 ultrasound software versions V1.0 through V4.0.0 due to incorrect calculation of Effective Regurgitant Orifice Area (EROA) when used with Fujifilm transducers, potentially leading to inaccurate heart flow measurements.
FujiFilmOct 14, 2021 - Use cautionMedical device
FujiFilm Healthcare Americas Corporation recalls Arietta 850 Ultrasound- Software Version: V1.0.0 through V4.1.3
Recalled FujiFilm Arietta 850 ultrasound systems with specific software versions (V1.0.0 to V4.1.3) may show incorrect mitral regurgitation and valve measurements, risking inaccurate cardiac diagnoses.
FujiFilmOct 14, 2021 - Lower riskMedical device
Beeken Biomedical, LLC recalls NuStat 8" x12" Trauma Pad XR Hemafiber, 5-pack. For temporary control of internal organ space bleeding REF: XR-0812-5
Beeken Biomedical recalls 5-pack NuStat 8"x12" Trauma Pads XR Hemafiber due to endotoxin levels exceeding safety limits for internal bleeding control.
Beeken BiomedicalOct 14, 2021 - Lower riskMedical device
Lumenis, Inc. recalls IPL Coupling Gel, I L (AX1009013), 12 pack of 0.25 L (AX1009018), 6 pack of 1 L (AX1009019 or AX1009063); and IPL
Lumenis recalls IPL coupling gels and devices due to potential bacterial contamination. FDA advises stopping use of Eco-Med ultrasound gels and lotions. Affected products include specific model numbers and packaging sizes.
LumenisOct 14, 2021 - Use cautionMedical device
SEDECAL SA recalls MobileDiagnost wDR, Model numbers 712001, 712002, 712004, 712006, and 712007
SEDECAL recalls MobileDiagnost wDR models 712001-712007 due to potential unintended movement if excessive liquid is used during cleaning, which could cause short circuits.
SEDECALOct 14, 2021 - Lower riskMedical device
Hill-Rom Inc. recalls These are communication systems, labeled as: a. NaviCare Nurse Call, Part Numbers: 3.6, 3.7, 3.9 b. Voalte Nurse Call,
Hill-Rom recalls specific nurse call communication systems due to potential failure during reboot cycles. Affected units may become non-functional and require replacement.
Hill-RomOct 14, 2021 - Lower riskMedical device
BioCheck, Inc. recalls T4 EIA Kit, Cat No: BC-1007, Store at 2-8C, For in vitro diagnostic use only This product s intended use is For the
BioCheck recalls T4 EIA Kit (BC-100: RN-60831/RN-60923) due to shelf-life issues causing failed controls. This affects in vitro diagnostic tests for thyroid disorders.
BioCheckOct 14, 2021 - UnratedDrug
Golden State Medical Supply Inc. recalls Ezetimibe and Simvastatin Tablets, 10 mg/40mg, a) 90 Tablets, b) 500 tablets, Rx only, Manufactured by Dr. Reddy's
Golden State Medical Supply recalls Ezetimibe and Simvastatin 10mg/40mg tablets due to foreign tablets found in some batches. This could cause harm if taken.
Golden State Medical SupplyOct 14, 2021 - Use cautionFood
KEURIG DR PEPPER recalls Target Good & Gather Coconut Pineapple Sparkling Water 8 pack of 12 oz. cans UPC can: 0 85239 04059 1, UPC outer carton
Target's Good & Gather Coconut Pineapple Sparkling Water is recalled due to unlabeled sulfites. Check your cans for the specific UPC and Best By date.
Good & GatherOct 14, 2021 - Stop using nowMeat & poultry
Butterball, LLC Recalls Ground Turkey Products Due to Possible Foreign Matter Contamination
Butterball recalls ~14,107 lbs of ground turkey due to possible blue plastic contamination. Check your freezer for affected lots and do not consume.
ButterballOct 13, 2021 - Use cautionVehicle
GENESIS GV80 (2021) recall — Seat Belts
Hyundai recalls 2021 Genesis GV80 vehicles with seat belt pretensioners that may explode in crashes, projecting metal fragments. Owners should contact Hyundai for free replacement.
HyundaiOct 13, 2021 - Use cautionVehicle
ZERO SR/F (2020) recall — Service Brakes, Hydraulic
Zero is recalling 2020 SR/F motorcycles with loose rear rotor bolts that could reduce braking and increase crash risk. Owners must have bolts tightened by dealers free of charge.
ZeroOct 13, 2021 - Use cautionVehicle
PORSCHE TAYCAN (2020) recall — Exterior Lighting
Porsche is recalling certain 2020-2021 Taycan vehicles due to hazard lights activating in non-emergency situations, which could confuse other drivers and increase crash risk. Owners should contact Porsche for free reprogramming.
PorscheOct 13, 2021 - Lower riskMedical device
Cook Inc. recalls Skinny Needle with Chiba Tip. RPN 090010, 090010-ET; GPN G14254, G15290. Rigid needle available with EchoTip to provide
Cook recalls Skinny Needle with Chiba Tip (RPN 090010, GPN G14254) due to potential black debris causing local inflammatory reactions. Affected units may need replacement.
CookOct 13, 2021 - UnratedMedical device
Elekta, Inc. recalls Oncentra Brachy users using version 4.0 and above with Applicator Modeling license 170283-00
Elekta recalls Oncentra Brachy software versions 4.0 and above with specific Applicator Modeling license (170283-00) due to potential dose delivery differences between planned and actual radiation treatment.
ElektaOct 13, 2021 - Lower riskMedical device
Instrumentation Laboratory recalls HemosIL ReadiPlasTin (20 mL), Part number 0020301400. An in vitro diagnostic thromboplastin reagent.
Instrumentation Laboratory recalls HemosIL ReadiPlasTin (20mL) lot N0705526 and N0806224 due to potential inaccurate test results. Affected users should check their product labels.
Instrumentation LaboratoryOct 13, 2021
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