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- Use cautionVehicle
FOREST RIVER BERKSHIRE (2021) recall — Equipment
Forest River is recalling 2021 Berkshire motorhomes with 3000W inverters that may cause fire due to overloaded wiring. Owners can get a free 2800W inverter replacement.
Forest RiverApr 9, 2020 - Use cautionVehicle
HYUNDAI TUCSON (2020) recall — Service Brakes, Hydraulic
Hyundai recalls 2019-2021 Tucson vehicles with potential engine compartment fire risk due to brake system corrosion. Free repairs include replacing HECU fuse and ESC software update. Owners advised to park away from structures until repairs.
HyundaiApr 9, 2020 - Lower riskMedical device
Wright Medical Technology Inc recalls WRIGHT INBONE Tibial Tray, Size: 2, Plasma Spray, Left, REF 2000252902 - Product Usage: is intended to give a patient
Wright Medical recalls a specific lot of INBONE Tibial Trays due to missing plasma coating. This may affect patient mobility and joint function. Contact for details.
Wright MedicalApr 9, 2020 - Lower riskMedical device
CooperSurgical, Inc. recalls CooperSurgical Dilator/Sound Set, Rx only, Sterile/EO, Made in South Korea, P/N MX21
CooperSurgical recalls sterile cervical dilator sets with potentially compromised pouch seals. Affected units from specific lot number may pose infection risk if used improperly.
CooperSurgicalApr 9, 2020 - Lower riskMedical device
The Binding Site Group, Ltd. recalls The Optilite Clinical Chemistry Analyzer. IVD. Model Number: IE700. UDI-05051700017176 - Product Usage: The Optilite
The Binding Site recalls The Optilite Clinical Chemistry Analyzer (model IE700) due to a software issue that may affect test result accuracy. Affected units run software versions 7.0 or 7.01.
The Binding SiteApr 9, 2020 - Use cautionMedical device
BD SWITZERLAND SARL recalls BD Alaris PCEA Administration Set, Microbore Tubing with Yellow Identification Stripe ASV, Catalog Number 30893-07 -
BD recalls Alaris PCEA Administration Sets with yellow tubing that may leak, causing under-infusion of medication and inadequate pain control. Affected units have specific catalog numbers and lot ranges.
BDApr 9, 2020 - Stop using nowConsumer product
Pass & Seymour Recalls Commercial-Grade Electrical Receptacles Due to Burn Hazard
Pass & Seymour recalls commercial-grade electrical receptacles with specific model numbers due to a burn risk when plugs are forced into the receptacle, causing overheating. Consumers should stop using and return for free replacement or refund.
Pass & SeymourApr 9, 2020 - Stop using nowConsumer product
Camso Recalls Yeti SnowMX Conversion Kits Due to Crash Hazard
Camso recalls Yeti SnowMX conversion kits (2018-2020) due to brake failure risk after installation. Consumers must stop using and get free repairs from authorized dealers.
YetiApr 9, 2020 - Use cautionVehicle
MERCEDES-BENZ SPRINTER (VS30) (2019) recall — Fuel System, Gasoline
Mercedes-Benz is recalling 2019 Sprinter vehicles with a potential fuel leak risk that could increase crash likelihood. Owners must have fuel pump nozzle checked by dealers.
Mercedes-BenzApr 8, 2020 - Use cautionVehicle
INDIAN SCOUT BOBBER (2019) recall — Service Brakes
Indian recalls 2019 Scout Bobbers with ABS brakes due to potential air in brake system reducing performance. Owners must have brakes serviced by dealers to prevent crash risk.
IndianApr 8, 2020 - Use cautionMedical device
Argon Medical Devices, Inc recalls PAC Tray/5 Catheter Introducer Tray 8F, Model 497424, Rx Only, STERILE EO, UDI: 00886333214440 - Product Usage: The
Argon Medical recalls PAC Tray/5 Catheter Introducer Tray 8F Model 497424 due to curved needle requiring needle driver, risking needle sticks during surgery.
Argon MedicalApr 8, 2020 - Lower riskMedical device
Qiagen Sciences LLC recalls therascreen EGFR RGQ PCR Kit (24), Reference Number REF 870121
Qiagen recalls Therascreen EGFR RGQ PCR Kit (24) due to rare false mutation positive results from fluorescence artefacts. All lots affected. No remedy specified.
QiagenApr 8, 2020 - Use cautionConsumer product
Continuum Recalls Lenox Tea Kettles Due to Burn Hazard
Continuum recalls Lenox 2:5 Quart tea kettles due to burn hazard from hot water expulsion. Consumers must stop using and get a refund.
LenoxApr 8, 2020 - Use cautionMedical device
Stryker Medical Division of Stryker Corporation recalls Stryker Power-PRO TL cot-powered ambulance cot Model Number 6550 - Product Usage: is a powered wheeled stretcher that
Stryker recalls Power-PRO TL ambulance cots (model 6550) that may not meet crash test standard BS EN 1789. Affected units include specific serial numbers listed in the recall notice.
StrykerApr 7, 2020 - Lower riskMedical device
Inpeco S.A. recalls FlexLab Automation System used with the following Modules: High Volume Storage(P/N FLX-270, FLX-271, FLX-276, FLX-282,
Inpeco recalls FlexLab automation systems with specific modules due to potential sensor delays that could cause safety issues in lab settings.
InpecoApr 7, 2020 - Lower riskMedical device
Innovasis, Inc recalls Oryx Cervical Screw Caddy, Model Number BTA-172, as part of the Oryx Cervical Plate System - Product Usage: The
Innovasis recalls Oryx Cervical Screw Caddy Model BTA-172 due to incorrect labeling of fixed and variable rescue screws, which could cause improper installation and interference with cover screws.
InnovasisApr 7, 2020 - Use cautionMedical device
Philips North America, LLC recalls Philips TraumaDiagnost- a Stationary X-Ray System (Bucky System) Model: 720013 - Product Usage: general radiography.
Philips recalls stationary X-ray system model 720013 due to risk of trauma arm falling if shaft breaks from material fatigue. Affected units have all serial numbers.
PhilipsApr 7, 2020 - Lower riskMedical device
Inpeco S.A. recalls Accelerator a3600 Automation System using the Aliquoter Module (Inpeco P/N FLX-212) - Product Usage: The systems
Inpeco recalls Accelerator a3600 Automation Systems with Aliquoter Module (P/N FLX-212) due to clot detection errors causing sample dilution. Affected units have specific serial numbers.
InpecoApr 7, 2020 - UnratedMedical device
Baxter Healthcare Corporation recalls Prismaflex Control Unit
Baxter Healthcare recalls Prismaflex Control Unit (Product Code 114870) due to lack of FDA clearance. Affected units may pose medical risks if used without proper regulatory approval.
Baxter HealthcareApr 7, 2020 - Lower riskMedical device
Inpeco S.A. recalls Accelerator a3600 Automation System with Advia2120LAS Interface Module (P/N FLX-219-00, FLX-219-10), ImmunoCAP 1000
Inpeco recalls Accelerator a3600 Automation System with specific interface modules due to a communication error causing sample tube misassociation. Affected units may require correction to prevent sample handling errors.
InpecoApr 7, 2020 - Lower riskMedical device
Inpeco S.A. recalls Inpeco FlexLab, ARCHITECT cSystem c8000/c16000 Interface Module, Part Numbers: FLX-208-00, FLX-208-10 - Product Usage:
Inpeco recalls specific FlexLab interface modules that may cause sample cross contamination if the carousel lid stays open or manual processing takes too long. Affected units include part numbers FLX-208-00 and FLX-208-10 with serial numbers listed.
InpecoApr 7, 2020 - Use cautionMedical device
Maquet Cardiovascular, LLC recalls HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-3 Branch, Product Code: M00202175912P0 - Product Usage: for use
Maquet recalls Hemashield Platinum Woven Double Velour Vascular Grafts with potential small holes at seam lines causing bleeding during surgery. Affected units have specific serial numbers.
MaquetApr 7, 2020 - Lower riskMedical device
Inpeco S.A. recalls Abbott Accelerator a3600 Centrifuge Module tube loading algorithm, Inpeco SA P/N: FLX-202, with Firmware Versions:
Inpeco recalls Abbott Accelerator a3600 Centrifuge Module with specific firmware versions and serial numbers due to potential unbalanced loads that could damage the centrifuge.
InpecoApr 7, 2020 - UnratedFood
H & C Food Inc. recalls Enoki Mushroom; 7.5oz (200g); UPC #831211204181; packed in clear plastic bag with green label; imported from Green Co.
H & C Food Inc. recalls Enoki mushrooms (7.5oz) from Feb 15-March 5, 2020, potentially contaminated with Listeria monocytogenes. Consumers should check UPC #831211204181 for affected items.
H & C Food Inc.Apr 7, 2020 - Use cautionVehicle
HONDA CLARITY ELECTRIC (2019) recall — Seat Belts
Honda is recalling 2019 Clarify Electric vehicles with rear seat belts that may not lock properly during crashes, increasing injury risk. Owners must contact Honda for free replacement.
HondaApr 6, 2020 - Use cautionVehicle
CHEVROLET SILVERADO 2500 (2020) recall — Structure
GM recalls 2020 Chevrolet Silverado 2500/3500 vehicles with improperly heat-treated hood striker wires that may fracture, causing unexpected hood openings while driving. Owners must have hood replaced free of charge.
ChevroletApr 6, 2020 - Lower riskMedical device
Agfa N.V. recalls AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic, Type number: 6010/200 - Product Usage: DR 800: Agfa
Agfa recalls DR 800 X-Ray systems with MUSICA Dynamic (Type 6010/200) due to potential incorrect dose calculations during fluoroscopy exams. Affected units have specific serial numbers; users should contact Agfa for details.
AgfaApr 6, 2020 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls System AXIOM Aristos FX - Product Usage: A dedicated x-ray system with a flat panel detector which allows the
Siemens recalls AXI: A dedicated x-ray system that may unintentionally expose patients to low radiation levels during rare unpressed exposure events. Affected units have serial numbers starting with 1192.
SiemensApr 6, 2020 - Use cautionMedical device
Philips North America, LLC recalls Philips Brilliance iCT SP Computed Tomography X-Ray System; Model # 728311
Philips recalls specific model of CT scanners due to potential cooling unit detachment risk. Affected units may require repair to prevent safety hazards.
PhilipsApr 6, 2020 - Use cautionMedical device
Skeletal Kinetics, Llc recalls OSTEOVATION EX, 5CC, IMPACT FORMULA. Product Number: 390-0205, UDI: 813845020047 - Product Usage: Callos is indicated
Skeletal Kinetics recalls OSTEOVATION EX 5CC Impact Formula for potential failure to maintain setting characteristics, risking longer surgery or incomplete bone healing. Affected units have specific lot numbers.
Skeletal KineticsApr 6, 2020
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