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
MERCEDES-BENZ SPRINTER 3500 (2018) recall — Electronic Stability Control (Esc)
Daimler Vans USA recalls 2012-2018 Mercedes-Benz Sprinter 3500 campers for potential Electronic Stability Control failure, increasing crash risk. Owners must contact DVUSA for free rear-wheel sensor replacement.
Mercedes-BenzMar 2, 2021 - Use cautionVehicle
LEXUS RX350 (2019) recall — Fuel System, Gasoline
Lexus recalls 2019 RX350 vehicles with potential fuel filler pipe fire risk during rear-end crashes. Owners must have transport hook inspected or removed by dealers.
LexusMar 2, 2021 - Use cautionVehicle
ROYAL ENFIELD INTERCEPTOR 650 (2020) recall — Service Brakes, Hydraulic
Royal Enfield is recalling 2018-2020 Interceptor 650 motorcycles due to corroded brake calipers that could reduce braking performance and increase crash risk. Owners will receive free caliper replacements.
Royal EnfieldMar 2, 2021 - Lower riskMedical device
AZURE BIOTECH INC recalls Assure COVID-19 IgG/IgM Rapid Test Device that include: 1) Pouch Label - FaStep Rapid Diagnostic Test *** Rapid
Azure Biotech recalls specific COVID-19 IgG/IgM Rapid Test Devices with incorrect labeling and unsupported 24-month expiration dating. Affected units may not be reliable for diagnostic use.
Azure BiotechMar 2, 2021 - Lower riskMedical device
Fujifilm Medical Systems U.S.A., Inc. recalls Synapse PACS - Radiological Image Processing System - Product Usage: intended for use, as a web based application, on
Fujifilm recalls Synapse PACS software versions 5.1 to 5.7.200 due to potential display of incorrect patient information in radiology systems.
Fujif: Medical SystemsMar 2, 2021 - Use cautionMedical device
Terumo Cardiovascular Systems Corporation recalls Consist of a distal connection mechanism (either standard Terumo Ball Quick Connect or Terumo Shaft Quick Connect), an
Terumo recalls specific stent retractors with potential stainless steel locking plates that could fracture, causing injury during surgery. Affected models include T401163 with serial numbers T00393-T00412.
TerumoMar 2, 2021 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls BCS XP System: Multipurpose system for in vitro coagulation studies. Product code: 10459330, 10461894, 10470625 -
Siemens Healthcare recalls BCS XP System units with product codes 10459330, 10461894, 10470625 due to potential emicizumab carryover in patient samples affecting coagulation test results.
Siemens HealthcareMar 2, 2021 - UnratedDrug
Ferring Pharmaceuticals Inc recalls Menopur 75 IU, (menotropins for injection), packaged as a) 5 single dose vials of Menotropins for injection, 5 single
Ferring Pharmaceuticals recalls Menopur 75 IU (menotropins for injection) due to failed pH specifications in 0.9% Sodium Chloride. This affects specific vial lots manufactured between 2020-2022.
FerringMar 2, 2021 - Lower riskDrug
Direct Rx recalls Nortriptyline HCL capsules, 10 mg, packaged in 30-count bottles, Rx only, Packaged and Distributed By: Direct Rx
Direct Rx recalls 10mg Nortriptyline capsules due to manufacturing errors affecting ingredient quality. Affected lots may contain incorrect active ingredient levels.
Direct RxMar 2, 2021 - Use cautionDrug
A-S Medication Solutions LLC. recalls Acetaminophen, Extra Strength, Aspirin Free, 500 MG Tablets, 100-count bottles, Mfr: Major Pharmaceuticals, Livonia, MI
A-S Medication Solutions recalls Health Essentials Kits containing Acetaminophen bottles with incorrect prescription drug labels. Check your kit's lot numbers.
A-S Medication SolutionsMar 2, 2021 - Lower riskFood
Flying Food Group LLC recalls Amazon Kitchen, Avocado Chicken Salad Sandwich, Net Wt. 8.1 oz., Cello wrap with cardboard liner, 1 unit per package,
Flying Food Group recalls Amazon Kitchen Avocado Chicken Salad Sandwich (8.1 oz) because soy allergen is undeclared on label. The product was made on shared equipment with foods containing soy. Consumers should check labels for soy allergen information.
Flying Food GroupMar 2, 2021 - Lower riskFood
Wilton Industries Inc recalls Wilton Rainbow Chip Crunch Sprinkles, 5.25 oz (148g) clear plastic bottle, SKU 710-5364 UPC 070896453648
Wilton recalls Rainbow Chip Crunch Sprinkles (5.25 oz clear plastic bottle) due to undeclared milk. Consumers should check product details and contact Wilton for guidance.
WiltonMar 2, 2021 - Lower riskFood
Canteen Inc. dba MG Foods, Inc. recalls MG Foods TURKEY & PROVOLONE BLT ON A BUTTERY CROISSANT, Net Wt. 8.1oz (229g), MG Foods Charlotte, NC 28208, UPC 1 00000
MG Foods recalls turkey and provolone BLT on butter croissant due to Listeria monocytogenes found in meat slicer environmental samples. Consumers should check UPC 1 00000 for affected products.
MG FoodsMar 2, 2021 - Lower riskMeat & poultry
Milky Way International Trading Corp. Recalls Canned Corned Beef Products Imported Without Benefit of Inspection
USDA FSIS recalls 297,715 pounds of canned corned beef imported without FSIS re-inspection. Consumers urged not to consume; products should be thrown away or returned.
MW PolarMar 1, 2021 - Use cautionMedical device
Brainlab AG recalls ExacTrac Dynamic (Medical Charged-Particle Radiation Therapy System).
Brainlab recalls ExacTrac Dynamic radiation therapy systems with software versions 1.0.0-1.0.2 due to potential unsafe patient positioning during treatment. Affected units may allow treatment to proceed when patient is out of safe range.
BrainlabMar 1, 2021 - Stop using nowMedical device
James Leckey Design Ltd recalls MyWay Walker Chassis - Product Usage: is intended for use by children already using a supportive walking device.
James Leckey recalls MyWay Walker Chassis units due to weld failures causing casters to detach. Check serial numbers and catalog codes for details.
James LeckeyMar 1, 2021 - Lower riskMedical device
Hitachi Medical Systems America Inc recalls Ultrasonic pulsed doppler imaging system - Product Usage: intended for use by trained personnel (doctor, Sonographer,
Hitachi Medical recalls Arietta 850 ultrasound software versions 4.0.0-4.0.2 with focus errors that may exceed regulatory acoustic limits when used with C252 probes.
Hitachi MedicalMar 1, 2021 - Lower riskMedical device
Abiomed, Inc. recalls Automated Impella Controller (AIC), Product No. 0042-0000-US, 0042-0010-US, 0042-0040-US. Used with Impella Ventricular
Abiomed recalls AIC controllers with software version 8.4 for potential pump recognition failure. Affected units require software update to prevent device malfunction.
AbiomedMar 1, 2021 - UnratedMedical device
Cellex recalls Cellex qSARS-Cov-2 Antigen Rapid Test, 25 tests/box, submitted as EUA202955 "declined to issue"
Cellex recalls 25-test antigen rapid tests due to lack of emergency use authorization. All units are affected. No remedy provided in official notice.
CellexMar 1, 2021 - Lower riskFood
B&G Sweet Heat Peppers recalls B&G Sweet Heat Pepper Dip, Ready To Eat, Refrigerated, packaged in 10 oz, semi-rigid plastic container. UPC 7 42832
B&G Sweet Heat Pepper Dip (10 oz) is recalled due to milk not being declared on label. This affects products with UPC 7 42832 sold before 3/5/2021. Consumers should check labels for missing milk declaration.
B&G Sweet Heat PeppersFeb 27, 2021 - Lower riskFood
Nutrin Distribution Co recalls Nutrin/Amendobras brand Roasted Peanut Splits packaged in 30lb cardboard boxes.
Nutrin Distribution Co recalls 30lb cardboard boxes of Roasted Peanut Splits due to possible Salmonella contamination. Consumers should check product labels for the recall number TOR0043/2:20.
NutrinFeb 27, 2021 - Stop using nowMeat & poultry
J&J Distributing Recalls Ready-to-Eat Meat and Poultry Salads and Wrap Products Due to Possible Listeria Contamination
J&J Distributing recalls 33 pounds of ready-to-eat meat and poultry salads and wraps from Feb. 2021 that may contain Listeria monocytogenes. Consumers are urged not to consume these products.
J&J DistributingFeb 26, 2021 - Use cautionVehicle
KTM 1290 SUPER DUKE R (2020) recall — Electrical System
KTM recalls 2020 1290 Super Duke R motorcycles with potentially incorrect rear wiring routing that could cause electrical short-circuits and crashes.
KTMFeb 26, 2021 - Use cautionMedical device
CAIRE DIAGNOSTICS INC recalls CAIRE DIAGNOSTICS FenomPro REF 900-0001 SN ***** - Product Usage: a portable, non-invasive device to measure fractional
CAIRE Diagnostics recalls FenomPro devices sold before Feb 2021 due to inaccurate FeNO readings that could lead to improper asthma management. Affected units have serial numbers 100107-100651.
CAIRE DiagnosticsFeb 26, 2021 - Lower riskMedical device
Hologic, Inc recalls Panther Fusion Tube Tray, REF PRD-04000, PN: FA-15004, Cont. 18 Tube Trays - Product Usage: an ancillary consumable to
Hologic recalls 18-count Panther Fusion Tube Trays (PN: FA-15004) that may leak, causing false positive/negative test results. Affected units sold with specific lot numbers.
HologicFeb 26, 2021 - Lower riskMedical device
Heartware, Inc. recalls Instructions for Use and Patient Manual for HeartWare HVAD System. Accompanies these system components: HVAD Sterile
Heartware recalls updated instructions for use and patient manuals for HVAD System components to address carrying case orientation, driveline cover safety, and power-up sequence clarity. These updates prevent potential misuse of the critical heart failure support device.
HeartwareFeb 26, 2021 - Lower riskMedical device
Stryker Corporation recalls Stryker, REF PC9001, PINPOINT Video Processor/Illuminator, Rx Only CE 0197, MD Medical Device, UDI: (01) 00858701006049
Stryker recalls PINPOINT Video Processor/Illuminators that may flicker, lose image, or reboot unexpectedly. This medical device is used with SPY-PHI and PINPOINT systems for imaging. Affected units have specific UDI codes.
StrykerFeb 26, 2021 - Use cautionMedical device
Covidien Llc recalls CF Delivery Dev Caps Bravo x5, FGS-0635/FGS 0636 - Product Usage: intended to be used for gastroesophageal pH
Covidien recalls CF Delivery Dev Caps Bravo x5 (FGS-0635/FGS-0636) for risk of capsule aspiration leading to low oxygen, intubation, and hospital stay. 13 reports of aspiration in 2 years.
CovidienFeb 26, 2021 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls Interventional Fluoroscopic X-Ray System - Product Usage: developed for single and biplane diagnostic imaging and
Siemens recalls certain interventional fluoroscopy systems that may randomly shut down due to UPS issues. Affected models include ARTIS Icono biplane and floor units. Consumers should contact Siemens for details.
SiemensFeb 26, 2021 - Lower riskMedical device
Heartware, Inc. recalls Medtronic HVAD Controller, Product Numbers: 1400, 1401, 1401AU, 1401BR, 1401CA, 1401CH, 1401DE, 1401GB, 1401IL, 1401IN,
Heartware recalls Medtronic HVAD Controller models 1400-1407 with potential port damage from cable misalignment. Affected users should contact Heartware for details.
HeartwareFeb 26, 2021
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