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
NISSAN PATHFINDER (2022) recall — Seats
Nissan recalls 2022 Pathfinder vehicles with third-row headrests that may move or detach during crashes, increasing injury risk. Owners must have headrests replaced free by dealers.
NissanSep 23, 2021 - Use cautionVehicle
CADILLAC ESCALADE (2021) recall — Fuel System, Gasoline
GM recalls 2021 Cadillac Escalades with faulty fuel pump power control module that may cause engine stalls and crashes. Get free replacement from dealers.
CadillacSep 23, 2021 - Use cautionVehicle
DRV MOBILE SUITE (2020) recall — Service Brakes, Hydraulic
DRV is recalling certain 2018-2021 Mobile Suites for potential brake caliper failure that could increase crash risk. Owners should contact dealers for free caliper clip replacement.
DRVSep 23, 2021 - Lower riskMedical device
Medtronic Neuromodulation recalls Clinician Programmer Application (CPA) model A610 Clinician Software Application
Medtronic recalls Clinician Programmer Application software versions 3.0.1048-1081 for potential software anomalies. Affected users should check their software version and contact Medtronic for updates.
Medtronic NeuromodulationSep 23, 2021 - Lower riskMedical device
DiaSorin Molecular LLC recalls SIMPLEXA COVID-19 Positive Control Pack, REF MOL4160, IVD, Rx Only, UDI: (01) 20816101027051
DiaSorin recalls SIMPLEXA COVID-19 Positive Control Packs with unapproved materials that may cause delayed amplification signals. Affected units include specific lot numbers and expiration dates.
DiaSorinSep 23, 2021 - Lower riskMedical device
Implant Direct Sybron Manufacturing LLC recalls ImplantDirect, REF 834713, Legacy 2 Implant 4.7mmD x 13mmL, 4.5mmD Platform,
Implant Direct recalls Legacy 2 dental implants that have incorrect size labeling compared to actual product. This mismatch could lead to improper fit during dental procedures.
Implant DirectSep 23, 2021 - UnratedDrug
Monarch PCM, LLC recalls Hydroquinone USP, 4% Skin Bleaching Cream, Rx only, Net Wt 1 oz (28.35g), Manufactured for: Westminster
Monarch PCM recalls 4% hydroquinone skin bleaching cream (Rx only) due to failing USP specifications. Affected units were manufactured for Westminster Pharmaceuticals in Nashville, TN. No remedy specified in recall notice.
Monarch PCMSep 23, 2021 - Stop using nowConsumer product
The Boppy Company Recalls Over 3 Million Original Newborn Loungers, Boppy Preferred Newborn Loungers and Pottery Barn Kids Boppy Newborn Loungers After 8 Infant Deaths; Suffocation Risk
Boppy recalls over 3 million newborn loungers due to suffocation risk from infants rolling or moving. 8 infant deaths linked to this hazard. Consumers must stop using and get refunds.
BoppySep 23, 2021 - Stop using nowConsumer product
Phoenix 200 All-Terrain Vehicles ATVs Recalled by Polaris Due to Crash Hazard (Recall Alert)
Polaris recalls 2011-2021 Phoenix 200 ATVs due to risk of throttle control breaking and causing crashes. Owners must stop using and get a free replacement bracket.
PolarisSep 23, 2021 - Use cautionVehicle
FORD EXPLORER (2013) recall — Suspension
Ford is recalling 2013 Explorer vehicles with a potential rear suspension toe link fracture risk due to a cross-axis ball joint (CABJ) that could seize. Owners must have their vehicles inspected by a dealer.
FordSep 22, 2021 - Use cautionVehicle
TOYOTA PRIUS (2022) recall — Engine And Engine Cooling
Toyota is recalling 2022 Prius vehicles with faulty engine software that may cause loss of drive power, increasing crash risk. Owners must update ECU software free of charge.
ToyotaSep 22, 2021 - Use cautionVehicle
FORD EXPLORER (2020) recall — Back Over Prevention
Ford recalls 2020-2021 Explorers with 360-degree cameras due to potential rearview camera image failure, increasing crash risk. Owners receive free software update.
FordSep 22, 2021 - Use cautionMedical device
Intuitive Surgical, Inc. recalls da Vinci SP Surgical systems with the following Model Name/ Model Number / UDI: ASSY,PSS,SP1098,P4/ 380601-44/
Intuitive Surgical recalls da Vinci SP Surgical systems with specific software versions that may experience energy delivery problems, requiring surgeon intervention or causing delays. Affected units include models with UDI codes listed in the recall notice.
Intuitive SurgicalSep 22, 2021 - Lower riskMedical device
Philips Healthcare recalls CombiDiagnost R90 is multi-functional general R/F systems.
Philips Healthcare recalls CombiDiagnost R90 medical devices due to missing required radiation labels, which could affect safety compliance. Affected units may need verification of labels.
Philips HealthcareSep 22, 2021 - Lower riskMedical device
RAYSEARCH LABORATORIES AB recalls RayStation/RayPlan versions 4 - 11A, including service packs. Build Stations: 4.0.0.14, 4.0.3.4, 4.3.0.14, 4.5.1.14,
RaySearch recalls software versions 4-11A with specific build numbers due to potential under/overestimation of radiation density in treatment planning. Affected users should check their version and contact RaySearch for updates.
RaySearchSep 22, 2021 - Use cautionMedical device
Z-Medica, LLC recalls QuikClot Combat Gauze-For Temporary External Use To Control Traumatic Bleeding Model / Part# 200
Z-Medica recalls QuikClot Combat Gau: Model 200 may have packaging seal breaches causing sterile barrier failure. Stop using if you own this product.
Z-MedicaSep 22, 2021 - Use cautionMedical device
MEDTECH SAS recalls ROSA One 3.1 Brain application The device is intended for the spatial positioning and orientation of instruments
MEDTECH SAS recalls ROSA One 3.1 Brain application software due to potential inaccurate electrode placement during brain surgery, risking serious injury or death. Affected units have specific serial numbers.
MEDTECH SASSep 22, 2021 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc recalls ADVIA Centaur SARS-CoV-2 Antigen Assay (100 Test Kit), SMN # 11207866
Siemens Healthcare recalls Centaur SARS-CoV-2 Antigen Test Kits (100 tests) due to insufficient validation data in EUA submission. Affected kits have specific lot numbers and expiration dates. Consumers should contact Siemens for details.
Siemens HealthcareSep 22, 2021 - Lower riskMedical device
bioMerieux, Inc. recalls VIDAS RUB IgG (RBG), REF 30226
bioMerieux recalls VIDAS RUB IgG (RBG) tests with specific lot numbers for potential delayed results due to a substrate error that prevents proper testing.
bioMerieuxSep 22, 2021 - UnratedDrug
SSM Health Care St. Louis DBA SSM St. Clare Health Center recalls Potassium Chloride 40 mEq in 0.9% Sodium Chloride 270 mL NS, 250 mL bag, Rx Only, SSM Health Care Corporation, 1015
SSM Health Care recalls Potassium Chloride 40 mEq in 0.9% Sodium Chloride 270mL bags due to lack of sterility assurance. This affects prescription-only products with specific NDC and lot numbers.
SSM Health CareSep 22, 2021 - Lower riskDrug
Teva Pharmaceuticals USA recalls AirDuo Digihaler 55/14 (fluticasone propionate 55 mcg and salmeterol 14 mcg) Inhalation Powder, Rx Only, Mktd by: Teva
Teva recalls AirDuo Digihaler 55/14 inhalers due to potential subpotent salmeterol levels. This may result in less effective treatment for asthma. Affected units have NDC 59310-111-06 and were manufactured in Ireland.
TevaSep 22, 2021 - UnratedDrug
New Vitalis Pharmacy LLC dba New Vitalis Pharmacy recalls Testosterone Cypionate Testosterone Propionate, 180mg/mL, 20mg/mL, 1 mL vial, Rx only, New Vitalis Pharmacy 4139
New Vitalis Pharmacy recalls specific testosterone vials (180mg/mL and 20mg/mL) for lack of sterility assurance. Affected lots expired by September 2021. Consumers should contact pharmacy for details.
New Vitalis PharmacySep 22, 2021 - Lower riskFood
Kelly's Bakery Corp. recalls Brownie Chocolate Walnuts, Carton with 96 retail units, A210107B
Kelly's Bakery recalls 96 units of Brownie Chocolate Walnuts due to undeclared walnuts on product labels. Consumers should check labels for the A210107B batch code.
Kelly's BakerySep 22, 2021 - Stop using nowFood
Whole Foods Market Brand 365, Llc recalls Whole Foods Market Everyday Double Crust Apple Pie sold in clear plastic clamshell with scale label applied. Sold as
Whole Foods Market recalls Everyday Double Crust Apple Pies due to undeclared milk and egg. Check PLUs and sell-by dates for details.
Whole Foods MarketSep 22, 2021 - Stop using nowConsumer product
Huish Outdoors Recalls Oceanic Adult Dry Top Snorkels Due to Drowning Hazard; Sold Exclusively at Costco
Oceanic recalls adult dry top snorkels with specific batch numbers due to a bottom purge valve leak that can cause unexpected water entry and drowning. Consumers must stop using and destroy the product to get a free replacement.
OceanicSep 22, 2021 - Use cautionVehicle
JEEP GRAND CHEROKEE (2021) recall — Visibility
Chrysler is recalling certain 2021 Jeep Grand Cherokee L vehicles due to a radio software error preventing rearview camera images from displaying, which could increase crash risk. Owners must update software for safety.
JeepSep 21, 2021 - Use cautionVehicle
RAM PROMASTER CITY (2020) recall — Exterior Lighting
Chrysler is recalling certain 2019-2021 Ram ProMaster City vehicles with turn signals that may not indicate failure to drivers, increasing crash risk. Owners must update BCM software for free.
ChryslerSep 21, 2021 - Lower riskMedical device
Philips Ultrasound Inc recalls EPIQ CVxi Diagnostic Ultrasound Systems, Product Code: 795232
Philips recalls EPIQ CVxi ultrasound systems with software versions 6.0, 7.0, 7.0.3 due to potential treatment delays from EchoNavigator errors. Affected units may require system restarts during certain procedures.
PhilipsSep 21, 2021 - Lower riskMedical device
Datascope Corp. recalls Cardiosave Li-Ion Battery Pack, Part No. 0146-00-0097. Component of the Cardiosave Hybrid Intra-Aortic Balloon Pump
Datascope recalls Cardiosave Li-Ion Battery Packs (Part No. 0146-00-0097) used in Cardiosave Hybrid and Rescue IABP models due to failing runtime tests. Affected units have specific model and serial numbers.
DatascopeSep 21, 2021 - Lower riskMedical device
Intuitive Surgical, Inc. recalls The da Vinci Xi and X surgical systems (IS4000 and IS4200) each consist of three main components: the Surgeon Console
Intuitive Surgical recalls da Vinci Xi and X surgical systems (IS40:000 and IS4200) due to incorrect expiration dates on packaging, which could lead to improper use of sterile components.
Intuitive SurgicalSep 21, 2021
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