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
35,004 found- Lower riskDrug
Contract Pharmacal Corporation recalls Major Extra Strength Acetaminophen Tablets, 500 mg Pain Reliever/Fever Reducer, packaged in a) 100-count bottles (NDC
Contract Pharmacal recalls 100-count and 1000-count acetaminophen tablets due to foreign tablets found in one bottle. Consumers should check product labels for NDC numbers.
Contract PharmacalFeb 3, 2020 - Use cautionVehicle
SUBARU LEGACY (2014) recall — Air Bags
Subaru is recalling 2014 Legacy vehicles with passenger air bag inflators that may explode due to propellant degradation from humidity and temperature. Owners must contact Subaru for free replacement.
SubaruFeb 1, 2020 - Stop using nowVehicle
SUBARU LEGACY (2014) recall — Air Bags
Subaru is recalling 2014 Legacy vehicles with passenger air bag inflators that may explode due to propellant degradation from humidity and temperature exposure, risking serious injury or death.
SubaruFeb 1, 2020 - Use cautionVehicle
SUBARU LEGACY (2014) recall — Air Bags
Subaru is recalling 2014 Legacy vehicles with passenger air bag inflators that may explode due to propellant degradation from humidity and temperature. Owners must contact Subaru for free replacement.
SubaruFeb 1, 2020 - Use cautionVehicle
VOLKSWAGEN ATLAS (2018) recall — Air Bags
Volkswagen recalls 2018 Atlas vehicles with faulty airbag sensors that may delay or disable deployment during crashes, increasing injury risk. Owners must have airbag sensor replaced free by dealers.
VolkswagenJan 31, 2020 - Lower riskMedical device
Cardinal Health 200, LLC recalls Presource Procedure Packs containing AAMI Level 3 surgical gowns, Multiple Catalog Numbers Produced Between September
Cardinal Health recalls Presource Procedure Packs containing AAMI Level 3 surgical gowns produced between September 2018 and January 2020. The gowns may not be sterile, increasing surgical site infection risk. Check catalog numbers and lot codes listed for affected items.
Cardinal HealthJan 31, 2020 - Lower riskMedical device
Hitachi Medical Systems America Inc recalls UST-2265-2 Probe, Part Number: UST-2265-2 - Product Usage: The UST-2265-2 probe is intended to be used for diagnostic
Hitachi Medical recalls 18 specific UST-2265-2 ultrasound probes due to potential miswiring in inner cables, which may cause lower peak velocity readings during diagnostic imaging. Affected units have unique serial numbers.
Hitachi MedicalJan 31, 2020 - Lower riskMedical device
Cardinal Health 200, LLC recalls Presource Procedure Packs containing AAMI Level 3 surgical gowns, Multiple Catalog Numbers Produced Between September
Cardinal Health recalls Presource Procedure Packs containing AAMI Level 3 surgical gowns produced between September 2018 and February 2020. The gowns may not be sterile, increasing surgical site infection risk. Affected kits include specific catalog numbers listed in the recall.
Cardinal HealthJan 31, 2020 - Use cautionMedical device
89 NORTH recalls LDI Laser firmware lower than V02.13.00 for LDI models: LDl-7, LDI-WF, LDI-NIR, LDl-6 Laser Science fluorescence imaging
89 NORTH recalls LDI Laser models with firmware versions older than V02.13.00 due to potential safety interlock failure. This could allow laser emission when safety interlocks are opened, violating federal regulations.
89 NORTHJan 31, 2020 - UnratedMedical device
Applied Medical Resources Corp recalls STEALTH SPRING CLIP 6mm latis (3/4 Force). REF/UDI::A1603/(01)00607915110581 - Product Usage: The device is indicated
Applied Medical Resources recalls STEALTH SPRING CLIP 6mm latis (3/4 Force) due to potential failure to properly clamp blood vessels during surgery, risking bleeding. Affected units have specific lot numbers and dates.
Applied Medical ResourcesJan 31, 2020 - UnratedDrug
Zydus Pharmaceuticals USA Inc recalls Ethacrynate Sodium for Injection, USP, 50mg/vial, Single Dose Vial, Rx Only, Manufactured by: Cadila Healthcare
Zydus Pharmaceuticals recalls 50mg/vial Ethacrynate Sodium injections due to cGMP deviations. Affected lots manufactured in India, distributed in US. Consumers should contact for details.
Zydus PharmaceuticalsJan 31, 2020 - Use cautionDrug
Efficient Laboratories, Inc. recalls New! Rompe Pecho MAX Multi Symptoms, 8 FL. Oz (237 mL) bottle, Distributed by: Efficient Laboratories, Inc. Miami, FL
Efficient Laboratories recalls New! Rompe Pecho MAX due to microbial contamination. Check lot 19B42, exp Feb 2022.
Efficient LaboratoriesJan 31, 2020 - Use cautionVehicle
CHEVROLET SILVERADO 1500 (2019) recall — Service Brakes, Hydraulic
GM recalls 2019 Chevrolet Silverado 1500 vehicles with potential electronic brake assist failure. Recalled vehicles may not comply with federal brake safety standards. Owners will receive free reprogramming of the EBCM.
ChevroletJan 30, 2020 - Use cautionVehicle
LAND ROVER DISCOVERY (2020) recall — Seats
Land Rover recalls 2020 Discovery vehicles with second row seat frames that may lack fasteners, risking occupant injury in crashes. Owners must have seats replaced by dealers.
Land RoverJan 30, 2020 - Use cautionVehicle
BMW X7 (2020) recall — Exterior Lighting
BMW recalls 2020 X7 models with faulty rear reflectors that reduce visibility to other drivers, increasing crash risk. Owners must have reflectors replaced free by dealers.
BMWJan 30, 2020 - Use cautionMedical device
Organ Recovery Systems, Inc. recalls LKT200 Perfusion Circuit, part of Lifeport Kidney Perfusion Transporter KTR - Product Usage: The circuit is an
Organ Recovery Systems recalls LKT200 Perfusion Circuits (Lots 119944, 119765, 119648, 120055, 120242) due to potential leakage at sample port assembly that could cause loss of perfusion solution needed for kidney transport.
Organ Recovery SystemsJan 30, 2020 - Lower riskMedical device
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls Medtronic CareLink 2090 Programmer. Used to interrogate and program Medtronic and Vitatron implantable devices, such as
Medtronic recalls CareLink 2090 Programmer devices with specific serial numbers due to two cyber vulnerabilities: improper access control and cleartext transmission of sensitive health information. Affected units may expose patient data to unauthorized access.
MedtronicJan 30, 2020 - Stop using nowConsumer product
Polaris Recalls Pro XD Utility Vehicles Due to Collision and Crash Hazards (Recall Alert)
Polaris recalls 2019 PRO XD UTVs with rear brake line puncture risk causing crashes. Owners must stop using and get free repairs from dealers.
PolarisJan 30, 2020 - Stop using nowConsumer product
Polaris Recalls Brutus Utility Vehicles (UTVs) Due to Collision and Crash Hazard (Recall Alert)
Polaris recalls 2017-2018 Brutus UTVs with rear brake line puncture risk causing brake failure. Affected vehicles have specific VIN ranges and model names. Owners must stop using and get repairs.
PolarisJan 30, 2020 - Stop using nowConsumer product
Pier 1 Recalls Desk Chairs Due to Fall and Injury Hazards
Pier 1 recalls upholstered swivel desk chairs from April to September 2019 due to risk of leg breakage causing falls and injuries. Consumers should stop using immediately and get a free repair kit.
Pier 1Jan 30, 2020 - Stop using nowConsumer product
K-Apparel Recalls Children’s Lounge Pants Due to Violation of Federal Flammability Standard; Burn Hazard (Recall Alert)
TINFL's children's lounge pants fail federal flammability standards, risking burns. Recalled items have specific lot numbers and sizes. Consumers should stop using and get refunds.
TINFLJan 30, 2020 - Stop using nowConsumer product
Bobcat Company Recalls Utility Vehicles (UTVs) Due to Collision and Crash Hazard (Recall Alert)
Bobcat recalls 2017-2018 3650 UTVs with rear brake line puncture risk. Stop using immediately and get free repair from dealer.
BobcatJan 30, 2020 - Use cautionMeat & poultry
Astrochef LLC. Recalls Pepperoni Stuffed Pizza Sandwich Products due to Misbranding and Undeclared Allergens
USDA FSIS recalls Astrochef pepperoni stuffed pizza sandwiches due to mislabeling and undeclared soy allergen. Consumers urged not to consume these products.
AstrochefJan 29, 2020 - Use cautionVehicle
FOREST RIVER VIBE (2020) recall — Service Brakes, Electric
Forest River recalls 2020 Vibe trailers due to potential brake failure if trailer separates from tow vehicle, increasing crash risk. Owners must replace break-away switch free of charge.
Forest RiverJan 29, 2020 - Lower riskMedical device
Fresenius Medical Care Holdings, Inc. recalls Honeywell Pressure Transducer- Part Number: 370506-22. It is a component used in 2008T, Common Name: Hemodialysis
Fresenius Medical Care is a leading global manufacturer of medical devices and healthcare products. We provide innovative solutions for dialysis, critical care, and other healthcare needs.
Fresenius Medical CareJan 29, 2020 - UnratedMedical device
Inova Lasers LLC recalls Class IV New Era medical laser device
Inova Lasers recalls Class IV New Era medical laser devices due to failure to meet electronic radiation control standards. Affected units may pose radiation risks if used improperly.
Inova LasersJan 29, 2020 - Lower riskMedical device
Beckman Coulter Inc. recalls ISE Electrolyte Reference (2 X 2L) Reagent, REF A28937, UDI: 15099590202491 - Product Usage: are intended for the
Beckman Coulter recalls ISE Electrolyte Reference reagents with low pH that may cause false high patient CO2 results, delaying treatment. Affected units have specific lot numbers and UDI codes.
Beckman CoulterJan 29, 2020 - UnratedMedical device
Abbott Vascular recalls NC TRAVELER Coronary Dilatation Catheter, REF 1013157-15, Rx Only,NC Traveler RX 4.0 X 15MM The NC Traveler RX Coronary
Abbott recalls NC Traveler Coronary Dilatation Catheters (REF 1013157-15) due to potential balloon deflation issues. This device is not cleared for U.S. distribution and may cause complications during procedures.
Abbott VascularJan 29, 2020 - UnratedDrug
UNICHEM PHARMACEUTICALS USA INC recalls Clonidine Hydrochloride Tablets, USP 0.1mg, Rx Only, 100-count bottle, Manufactured by: Unichem Laboratories Ltd.
Unichem recalls 19,161,600 bottles of Clonidine Hydrochloride 0.1mg tablets due to potential Benzophenone migration from container labels.
Unichem PharmaceuticalsJan 29, 2020 - Lower riskFood
Salud Natural Entrepreneur, Inc. recalls Nopalina Flax Seed Fiber in 1 and 2 lb bags, UPC 8 90523 00072 0 and 8 90523 00084 3
Salud Natural recalls Nopalina Flax Seed Fiber products due to Salmonella contamination. Products sold with specific UPCs and lot numbers from 2021 are affected. Consumers should check labels for affected items.
Salud NaturalJan 29, 2020
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