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
34,943 found- Stop using nowVehicle
HONDA GL1800 (2016) recall — Air Bags
Honda is recalling 2016 GL1800 Gold Wing motorcycles with air bag modules that may explode due to propellant degradation, risking serious injury or death. Owners must contact Honda for free replacement.
HondaSep 1, 2018 - Stop using nowMeat & poultry
J.T.M. Provisions Company Recalls Cooked Ground Beef Products Due To Possible Listeria Contamination
J.T.M. Provisions recalls cooked ground beef patty crumbles due to possible Listeria monocytogenes contamination. Do not consume; discard or return immediately.
J.T.M. ProvisionsAug 31, 2018 - Use cautionVehicle
FORD F-150 (2018) recall — Seat Belts
Ford is recalling 2015-2018 F-150s with seat belt pretensioner issues that could cause vehicle fires if materials ignite during crashes.
FordAug 31, 2018 - Use cautionVehicle
FCCC XBR (2018) recall — Exterior Lighting
Daimler Trucks North America recalls 2016-2019 FCCO XBR vehicles with potentially nonfunctioning rear lights. This recall addresses a risk of crashes due to malfunctioning brake, turn, or marker lights.
Daimler Trucks North AmericaAug 31, 2018 - Lower riskMedical device
Terumo Cardiovascular Systems Corporation recalls VirtuoSaph Plus Endoscopic Vessel Harvesting System, Catalog Number: VSP550EX Product Usage: The VittuoSaph¿ Plus
Terumo recalls VirtuoSaph Plus Endoscopic Vessel Harvesting System (VSP550EX) due to a generator compatibility issue that could affect surgical safety. Affected units may require specific generator checks.
TerumoAug 31, 2018 - Lower riskMedical device
Accuray Incorporated recalls Ashland(TM) Box Film Ball Cube II EBT3, P/N: 027863-002 rev E Product is used to calibrate CyberKnife systems
Ashland Box Film Ball Cube II EBT3 calibration film (P/N 027863-002 rev E) sold between Aug 2017-July 2018 may cause up to 0.5mm positional error in CyberKnife systems. Affected units should be checked for model and serial number.
AshlandAug 31, 2018 - Lower riskMedical device
GE Healthcare, LLC recalls Dash 5000 Patient Monitoring System is used to monitor physiologic parameter data on adult, pediatric and neonatal
GE Healthcare recalls Dash 5000 Patient Monitoring Systems that may restart simultaneously during network overload, potentially disrupting patient monitoring. Affected units were sold from 2019 to 2023.
GE HealthcareAug 31, 2018 - Stop using nowMedical device
Widex A/S recalls Widex BABY hearing aid (referred to as BABY440), powered by zinc-air batteries size 10 Intended use: BABY440 is
Widex recalls a small number of BABY440 hearing aids due to a non-tamper-resistant battery drawer. Check your serial number for details.
WidexAug 31, 2018 - Use cautionDrug
Beaumont Bio-med, Inc. recalls Skin Irritation & Itch Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed
Beaumont Bio-med recalls 192 bottles of Skin Irritation & Itch Response Homeopathic Formula due to potential microbial contamination from CGMP deviations.
Beaumont Bio-medAug 31, 2018 - Lower riskDrug
BioLyte Laboratories, LLC recalls NeoRelief for Muscle Cramping & Restlessness Homeopathic Topical Gel, packaged in a) 4 ml sample packs and b) Net Wt.
BioLyte recalls NeoRelief topical gel due to water contamination in some batches. Products with specific lot numbers and expiration dates are affected. Consumers should check labels for recalled lots.
BioLyteAug 31, 2018 - Use cautionMeat & poultry
Publix Super Markets Inc. Recalls Ground Chuck Products Due To Possible E. coli O26 Contamination
Publix is recalling ground beef products purchased between June 25 and July 31, 2018, due to possible E. coli O26 contamination. Consumers are urged not to consume these products and should throw them away or return to store.
PublixAug 30, 2018 - Use cautionVehicle
CHAMPION CHALLENGER (2014) recall — Equipment Adaptive/Mobility
Champion is recalling 2012-2018 Challenger vehicles with certain wheelchair lifts due to risk of wheelchair user tipping into vehicle during exit. Owners must have lift replaced with safer cam.
ChampionAug 30, 2018 - Use cautionVehicle
CHEVROLET SILVERADO 2500 (2016) recall — Service Brakes, Hydraulic
Chevrolet is recalling 2016 Silverado 2500 vehicles with loose brake pedal pivot nuts that could cause loss of braking power. Owners must contact GM for free repairs to prevent crash risks.
ChevroletAug 30, 2018 - Use cautionVehicle
KAWASAKI NINJA (2018) recall — Structure
Kawasaki recalls 2018 Ninja H2 SX SE motorcycles with a center stand that may unexpectedly drop, causing loss of control and crashes. Owners must contact dealers for free replacement of the left center stand bracket.
KawasakiAug 30, 2018 - Use cautionVehicle
JAYCO ALANTE (2018) recall — Suspension
Jayco recalls 2018 Alante vehicles with damaged hydraulic hoses that may leak fluid, risking fire if it contacts exhaust. Owners must have hoses inspected and replaced free by dealers.
JaycoAug 30, 2018 - Use cautionVehicle
FREIGHTLINER CASCADIA (2019) recall — Engine And Engine Cooling
Daimler Trucks recalls 2019 Freightliner Cascadia trucks with potential fuel line bursts causing leaks and engine stalling. Owners must contact DTNA for free steel fuel line replacement.
Daimler TrucksAug 30, 2018 - Use cautionVehicle
BUICK LACROSSE (2019) recall — Service Brakes, Hydraulic
GM recalls 2019 Buick Lacrosse with potential brake performance issues that could increase crash risk. Owners should contact GM for free brake system bleeding.
BuickAug 30, 2018 - Lower riskMedical device
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls Mitek Screw and Washer Depth Gauge, Product Code 219024
DePuy Mitek recalls screw and washer depth gauges with a 3.2mm reading error that may lead to incorrect bone hole measurements during surgery.
DePuy MitekAug 30, 2018 - Lower riskMedical device
Arrow International Inc recalls Arrow AGB + Multi-Lumen CVC Kit, Cat. No. CDC-42703-B1A. Product Usage - The Arrow CVC is intended to provide
Arrow recalls CVC kits with expired dates due to shipping errors. Using expired kits may affect sterility or function. Check product labels for expiration date.
ArrowAug 30, 2018 - Lower riskMedical device
Mindray DS USA, Inc. dba Mindray North America recalls Mindray BeneVision Distributed Monitoring System (DMS), Part No. 115-034413-00
Mindray recalls BeneVision DMS software versions 03.01.00 to 03.03.00 due to ECG waveforms showing flat lines when more than 64 TD60 transmitters are connected to a central station.
MindrayAug 30, 2018 - Lower riskMedical device
Becton Dickinson & Company recalls BD Vacutainer Urine Collection Cups, Cat. No. 364941
BD Vacut: Urine collection cups may cause slight red blood cell elevation when used with Sysmex analyzers. Follow GCP guidelines for urine testing to ensure accurate results.
Becton DickinsonAug 30, 2018 - Lower riskMedical device
MEDLINE INDUSTRIES INC recalls Unna-Z: Unna Boot Compression Wrap with Zinc Oxide and Calamine, Item Numbers: a) NONUNNA3 and b) NONUNNA4 Product is
Medline recalls Unna-Z compression wraps with zinc oxide and calamine due to mold in specific lots. Affected items have item numbers NONUNNA3 or NONUNNA4 and certain lot numbers. Consumers should check their product details.
MedlineAug 30, 2018 - Lower riskMedical device
GE Healthcare, LLC recalls Centricity Universal Viewer with Cross Enterprise Display This impacts product versions 6.0 SP1 and higher.
GE Healthcare recalls Centric: Universal Viewer versions 6.0 SP1+ due to potential wrong patient displays without caution icons. Affected users should check system ID and UDI numbers.
GE HealthcareAug 30, 2018 - Lower riskMedical device
Medtronic Navigation, Inc.-Littleton recalls O-arm 1000 2nd Edition Imaging System, OARM ASSY Bl70000027 SYSTEM PRODUCT, Model Number Bl70000027 Product Usage: The
Medtronic recalls O-arm 1000 2nd Edition Imaging Systems with software anomalies affecting startup, shutdown, communication, motion control, and imaging functions. Update to software version 3.1.7 resolves the issue.
MedtronicAug 30, 2018 - Lower riskDrug
Alkano Chemicals, Inc recalls Thyroid powder, 4.5 kg foil bag, 5x1 kg foil bags packed in 25 Kg Fiber Drum, Thyroid Powder 25kg/drum, US
Alkano Chemicals recalls thyroid powder due to inconsistent levothyroxine and liothyronine levels. Affected products were sold in 25kg fiber drums with specific NDC and lot numbers.
Alkano ChemicalsAug 30, 2018 - Stop using nowConsumer product
PetSmart Recalls Strip Lights for Reptile Cages Due to Fire Hazard
PetSmart recalls 20" and :30" reptile strip lights due to fire risk from overheating bulbs. Stop using immediately and return for refund.
PetSmartAug 30, 2018 - Stop using nowConsumer product
Core Health & Fitness Recalls Stairmaster Stepmill Exercise Equipment Due to Fall Hazard (Recall Alert)
Recall of StairMaster 8G Gauntlet Stepmill machines with model numbers 9-5250 & 9-5270 due to fall hazard from rapid step acceleration. Consumers must stop using and contact for free repair.
Core Health & FitnessAug 30, 2018 - Lower riskMeat & poultry
Olufela Yemitan Recalls Siluriformes Products Distributed Without Benefit of Import Inspection
USDA FSIS recalls 45 pounds of smoked Siluriformes products imported from Nigeria without U.S. inspection due to ineligible country. Consumers urged not to consume and dispose of items.
Olufela YemitanAug 29, 2018 - Lower riskMeat & poultry
Taylor Farms Illinois, Inc. Recalls Beef and Pork Meatloaf Products Due To Misbranding and Undeclared Allergens
USDA recalls Taylor Farms beef and pork meatloaf products due to undeclared allergens (eggs, wheat) that may cause allergic reactions. Consumers urged to discard products.
Taylor FarmsAug 29, 2018 - Use cautionVehicle
TOYOTA AVALON (2012) recall — Air Bags
Toyota recalls 2012 Avalon vehicles with seat belt assemblies that may incorrectly signal air bags as buckled, risking injury in crashes. Owners should contact Toyota for free testing or replacement.
ToyotaAug 29, 2018
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