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
35,069 found- Use cautionMedical device
B. Braun Medical, Inc. recalls Dispensing Pins for Air Inlet Filter, Product Catalog No. 412005, DP2500 Dispensing Pin W/Valve. A valve for aspiration
B. Braun recalls DP2500 Dispensing Pins with potential leakage risk that could cause medication dose errors or bloodstream infections. Affected units have specific lot numbers and expiration dates.
B. BraunJan 31, 2022 - Stop using nowMeat & poultry
FSIS Issues Public Health Alert for Ready-To-Eat Chicken Salad Products Due to Possible Listeria Contamination
Public Health Alert for Simply Fresh Market RTE chicken salad (Apples & Walnuts) due to possible Listeria monocytogenes contamination. Do not consume.
Simply Fresh MarketJan 28, 2022 - Use cautionVehicle
FOREST RIVER VENGEANCE (2022) recall — Tires
Forest River recalls 2022 Vengeance Fifth Wheel trailers with incorrect tire pressure labels that may cause under-inflated tires and crash risk. Owners receive free replacement labels.
Forest RiverJan 28, 2022 - Use cautionVehicle
PORSCHE CAYENNE (2021) recall — Suspension
Porsche is recalling certain 2021 Cayenne vehicles due to rear axle misalignment causing uneven tire wear, which increases crash risk. Owners must have rear axle inspected and tires replaced if needed at no cost.
PorscheJan 28, 2022 - Use cautionVehicle
GRAND DESIGN IMAGINE (2020) recall — Structure
Grand Design is recalling 2020-2021 Imagine travel trailers with potentially sharp handle edges that could cause cuts. Owners should contact customer service for free handle replacements.
Grand DesignJan 28, 2022 - Use cautionVehicle
GRAND DESIGN REFLECTION (2020) recall — Equipment
Grand Design is recalling certain 2013-2021 Reflection RVs due to a 110-volt wire that may cause electrical arcs and fire. Owners should contact customer service for free wiring repairs.
Grand DesignJan 28, 2022 - Use cautionMedical device
GE Healthcare, LLC recalls GE Healthcare CARESCAPE Central Station (CSCS) V2.0x MAI700 (Integrated), REF 2082278-001, and MAS700 (Desktop, REF
GE Healthcare recalls v2.0 Central Station models with unapproved keyboards that may mute alarms, risking missed critical alerts. Affected units include specific serial numbers and versions.
GE HealthcareJan 28, 2022 - UnratedMedical device
Remote Diagnostic Technologies Ltd. recalls Tempus LS, Type DGE1, CAT 00-3010, REF 3.940590, Software version 1.3.5, UDI: (01)07613365001693
Remote Diagnostic Technologies recalls Tempus LS defibrillators with specific software and serial numbers due to not being approved for US distribution. Affected units may pose safety risks.
Remote Diagnostic TechnologiesJan 28, 2022 - Lower riskMedical device
Brasseler USA, Medical L.L.C. recalls Brasseler USA, K-WIRE, Double Trocar Smooth, REF KM172-26-35S
Brasseler USA recalls K-WIRE Double Trocar Smooth (Lot NV1MX) due to unsealed packaging. Consumers should check product labels for the lot code to determine if affected.
Brasseler USAJan 28, 2022 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Siemens Dimension Vista Magnesium Flex reagent cartridge (MG) Material # 10445158, Catalog # K3057 used in the
Siemens recalls Magnesium Flex reagent cartridges (Material #10445158) that may cause QC failures or incorrect patient results. Affected lots include 21253BB, 21263BA, and 21335AA. Contact Siemens for remedy.
SiemensJan 28, 2022 - Stop using nowMedical device
Sam Medical Products recalls SAM CHEST SEAL REF CS203-EN Combo LOT Y060321-09
Sam Medical Products recalls CS203-EN Combo chest seal lot Y060321-09 due to a hole in the dressing that prevents creating an occlusive seal over chest wounds. Affected units may not function correctly in emergencies.
Sam Medical ProductsJan 28, 2022 - Use cautionMedical device
B Braun Medical Inc recalls Conductivity Sensors utilized on Dialog and Dialog+ Hemodialysis Systems. Conductivity Sensor (END) - VERSION 2,
B Braun Medical recalls Conductivity Sensors (VERSION 2) for Dialog and Dialog+ hemodialysis systems due to potential cracks causing leaks that may lead to improper ultrafiltration. Affected units include specific model numbers and lots.
B Braun MedicalJan 28, 2022 - Stop using nowDrug
Esupplementsales, LLC recalls HARD DAWN, Rise and Shine capsules, 500 mg, packaged in 10-count blisters per carton, Made in Malaysia, UPC 680044
Esupplementsales recalls HARD DAWN Rise and Shine 500mg capsules due to unapproved drug content. Analytical testing found tadalafil, a FDA-approved drug, making this product unapproved. Consumers should stop using immediately.
EsupplementsalesJan 28, 2022 - Lower riskDrug
AMS Packaging Inc recalls Premium Nature Instant Hand Sanitizer, (ethyl alcohol 70%), plastic bottle packaged as (a) 8 OZ, UPC 8 19192 02866 8;
FDA found some Premium Nature hand sanitizer bottles have less than 70% ethanol. Consumers should check UPCs and stop using affected products.
Premium NatureJan 28, 2022 - UnratedFood
CONAGRA BRANDS recalls Wishbone Chunky Blue Cheese Dressing 24oz. bottle UPC 0-41321-00691-3; six bottles per case
Conagra Brands recalls Wishbone Chunky Blue Cheese Dressing 24oz bottles with undeclared eggs. Consumers should check UPC 0-41321-00691-3 and lot number 4254201320 (NOV0922).
Conagra BrandsJan 28, 2022 - Use cautionConsumer product
Johnson Health Tech Recalls Matrix T1 and T3 Commercial Treadmills Due to Fire Hazard (Recall Alert)
Johnson Health Tech recalls Matrix T1 and T3 commercial treadmills due to fire risk from loose power cords. Affected units have specific serial numbers and were sold from 2009-2018. Contact for free power cord bracket installation.
Johnson Health TechJan 28, 2022 - Use cautionVehicle
CADILLAC ESCALADE (2021) recall — Power Train
General Motors recalls 2021 Cadillac Escalade vehicles with potentially unsafe rear driveshaft assemblies that could cause sudden power loss and crash risk. Owners must contact dealers for free replacement.
CadillacJan 27, 2022 - Use cautionVehicle
TESLA MODEL 3 (2020) recall — Electrical System
Tesla is recalling 2020 Model 3 vehicles with rolling stop feature that may not stop at stop signs, increasing crash risk. Owners must update software to disable the feature.
TeslaJan 27, 2022 - Use cautionVehicle
RAM 2500 (2020) recall — Visibility
Chrysler recalls 2019-2020 RAM 2500 models with potential wiper arm looseness causing reduced visibility. Owners must contact FCA US, LLC for free wiper nut tightening.
RAMJan 27, 2022 - Use cautionMedical device
Medtronic MiniMed recalls MiniMed 630G: MMT-1715, MMT-1754, MMT-1755; MiniMed 670G: MMT-1740, MMT-1741, MMT-1742, MMT-1760, MMT-1761, MMT-1762,
Medtronic MiniMed 630G and 670G insulin pumps sold in last 6 months may not deliver basal insulin without proper setup, risking severe hyperglycemia and diabetic ketoacidosis. Affected units have serial numbers from NG2056884H to NG2891033H (US) or NG1921788H to NG2883091 (OUS).
Medtronic MiniMedJan 27, 2022 - Stop using nowMedical device
IN MY BATHROOM LLC recalls The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak
IN MY BATHROOM LLC recalls handheld UV-C germicidal wands (Model Seago SG-153) due to excessive UV-C radiation risk. Consumers should stop using the product immediately.
IN MY BATHROOM LLCJan 27, 2022 - Lower riskMedical device
Hologic, Inc recalls Panther Fusion Extraction Reagent-X, REF PRD-04477, For use with Panther Fusion System, IVD, Rx only, Contents: FCR-X
Hologic recalls Panther Fusion Extraction Reagent-X (lot 281375, 291829) due to potential false negative test results. Affected kits may not detect diseases correctly.
HologicJan 27, 2022 - Lower riskMedical device
Heartware, Inc. recalls HeartWare Ventricular Assist Device (HVAD) System
Heartware recalls specific HVAD system models for updated cleaning instructions to avoid removing lubricant from power connector pins, which could cause power switching issues.
HeartwareJan 27, 2022 - Stop using nowMedical device
Integrity Implants Inc. recalls LineSider Spinal System 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Cannulated. Thoracolumbosacral pedicle screw
Integrity Implants recalls LineSider Spinal System screws for potential weld separation between components, which could lead to failure during spinal surgery. Affected units include specific sizes and lot numbers.
Integrity ImplantsJan 27, 2022 - Lower riskMedical device
E25Bio, Inc. recalls E25Bio COVID-19 Direct Antigen Rapid Test ; E25Bio COVID-19 DART Kit
E25Bio recalls its COVID-19 Direct Antigen Rapid Test kits as they were distributed without FDA authorization for clinical use. Consumers should not use these products for testing.
E25BioJan 27, 2022 - Use cautionMedical device
C.R. Bard Inc recalls BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS14C
Bard recalls 14Fr SURESTEP intermittent catheter trays with potential leak at catheter-drain bag connection. Affected units have specific serial numbers. Stop using immediately to prevent leaks.
BardJan 27, 2022 - Use cautionVehicle
PIERCE ARROW XT (2016) recall — Fuel System, Diesel
Pierce recalls 2015-2021 Arrow XT fire trucks due to potential fuel leaks causing fire. Owners with 75 miles or less need vibration isolators; older models get new fuel tubes. Notification mailed March 11, 2022.
PierceJan 26, 2022 - Use cautionVehicle
TOYOTA VENZA HYBRID (2021) recall — Exterior Lighting
Toyota recalls 2021 Venza Hybrids due to water entering rear turn signal lights causing short circuits and potential crash risks. Owners must have bulbs replaced by dealers by June 30, 2022.
ToyotaJan 26, 2022 - Use cautionVehicle
AUDI A4 ALLROAD (2020) recall — Tires
Audi is recalling 2020 A4 Allroad vehicles with rear axle misalignment that may cause uneven tire wear and crash risk. Owners must get free rear axle inspection and tire replacement.
AudiJan 26, 2022 - Stop using nowDrug
AuroMedics Pharma LLC recalls Polymyxin B for Injection USP, 500,000 Units per Vial, 10 mL vials, packaged in 10 vials per carton, Sterile, Rx Only,
AuroMedics Pharma recalls Polymyxin B for Injection due to hair discovered in vials. This sterile prescription drug (NDC 55150-234-10) may contain particulate matter. Affected lots: CPB200013 (exp 9/2022).
AuroMedicsJan 26, 2022
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83,807 recalls tracked · 72,041 explained in plain English · 10,992 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.