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
35,021 found- Use cautionVehicle
LUCID AIR (2025) recall — Electrical System
Lucid is recalling certain 2022-2026 Air vehicles due to overheated electrical circuits that could cause fire or reduce visibility. Owners must park outside until software update is applied.
LucidAug 21, 2026 - Stop using nowMedical device
Medtronic MiniMed, Inc. recalls Brand Name: MiniMed Flex Product Name: MiniMed Flex Insulin Pump Model/Catalog Numbers: MMT-8062; MMT-8072 Product
Medtronic recalls MiniMed Flex insulin pumps (MMT-8062/8072) due to failed verification tests that may cause inaccurate insulin delivery or device failure.
MiniMedAug 20, 2026 - Use cautionMedical device
Heraeus Medical GmbH (Dental Division) recalls PALACOS MV+G pro 40; PALACOS MV+G pro 80. Model/Catalog Number: 5081290; 5081291. Radiopaque, poly(methyl
Heraeus Medical recalls PALACOS MV+G pro 40 dental bone cement (model 5081290) due to potential monomer leakage. All units sold worldwide from 2026-08-20 are affected. Return or stop use immediately.
Heraeus MedicalAug 20, 2026 - Use cautionMedical device
Bard Peripheral Vascular Inc recalls EnCor EnCompass Breast Biopsy and Tissue Removal System Console (model number: ENCPCONSOLE) and Driver (model number:
Bard Peripheral Vascular Inc recalls EnCor EnCompass Breast Biopsy and Tissue Removal System Console and Driver with specific software versions and serial numbers due to potential calibration errors that could interrupt procedures or require repeat biopsies.
Bard Peripheral VascularAug 20, 2026 - Lower riskMedical device
Alere San Diego, Inc. recalls Fisher Scientific Sure-Vue Serum/Urine hCG, Model/ Part: FHC-202/23900529, FHC-202/23900528; Beckman Coulter Inc's ICON
Alere recalls hCG pregnancy tests that may detect low hCG levels, causing false positives. Affected products include Sure-Vue and ICON tests with specific model numbers and dates.
AlereAug 20, 2026 - Use cautionFood
Admiral Beverage Corporation recalls 7up Tropical beverage, shelf stable, 12oz can in a 12pk wrap, labeled as 7 up Tropical Beverage containing cans that
Admiral Beverage recalls 7up Tropical cans labeled as Zero Sugar that contain full sugar. Check your UPC and lot code for details.
7upAug 20, 2026 - Lower riskMedical device
DeRoyal Industries Inc recalls REF: 81-030415 Myocardial Probe Non-Pyrogenic , 400 Series
DeRoyal recalls 400 Series Myocardial Probes with 18mm needle instead of 15mm. This incorrect size may cause injury during medical procedures. Affected units sold with specific lot numbers.
DeRoyalAug 20, 2026 - UnratedDrug
Sterling Pharmaceutical Services LLC recalls TRP The Relief Products* Gentle Eyes Lubricant Eye Drops, Carboxymethylcellulose sodium 0.5%, Sterile Eye Drops, 0.5 FL
Sterling Pharmaceutical Services LLC recalls TRP Gentle Eyes Lubricant Eye Drops due to lack of assurance of sterility. This could pose a risk of infection. Consumers should contact the manufacturer for details.
TRP The Relief ProductsAug 20, 2026 - Use cautionMedical device
ICU Medical, Inc. recalls CADD Yellow Medication Cassette Reservoir with NRFit connector US Product Codes: 21-7600-24, 21-7609-24 OUS Product
ICU Medical recalls CADD Yellow Medication Cassette Reservoirs with NRFit connector due to potential medication leakage at the joint, which could cause therapy delays, medication exposure, or air embolus.
ICU MedicalAug 20, 2026 - Lower riskMedical device
Wilson-Cook Medical Inc. recalls Brand Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Product Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Model/Catalog Number: HEMO-7,
Wilson-Cook Medical recalls HEMOSPRAY Endoscopic Hemostats (models HEMO-7, HEMO-10, HEMO-7-EU, HEMO-10-EU) due to endoscope adherence and inability to spray powder. The firm will provide an updated Instruction for Use.
HEMOSPRAYAug 20, 2026 - Use cautionVehicle
BUICK ENCORE GX (2025) recall — Back Over Prevention
General Motors recalls 2025 Buick Encore GX vehicles with rearview camera that may display distorted or blank images, increasing crash risk. Owners must contact dealers for free camera replacement.
BuickAug 20, 2026 - Stop using nowConsumer product
Workbless Pressure Washers Recalled Due to Risk of Serious Injury or Death from Shock and Electrocution Hazards
Workbless WB0301 and WB0302 pressure washers lack GFCI protection. Stop using them now and contact Workbless for a full refund.
WorkblessAug 20, 2026 - Stop using nowConsumer product
Modine Manufacturing Company Recalls Airedale Heating and Cooling Ventilation Fans Due to Fire Hazard
Modine recalls Airedale ClassMate and SchoolMate heat pumps due to fire hazard. Stop using immediately and contact Modine for free inspection.
AiredaleAug 20, 2026 - Stop using nowConsumer product
KTM North America Recalls Off-Road Motorcycles Due to Risk of Serious Injury or Death from Crash Hazard
Recalled 2021-2024 off-road motorcycles (GASGAS and Husqvarna) have rear brake calipers that can crack or break, risking serious injury or death. Consumers must stop riding and get free repairs at authorized dealers.
GASGAS & HusqvarnaAug 20, 2026 - Stop using nowConsumer product
Koorlian Mattresses Recalled Due to Risk of Serious Injury or Death from Fire Hazard; Violate Mandatory Standard for Mattress Flammability; Sold on Amazon by Dream Bedding Technology
Koorlian mattresses sold on Amazon by Dreams Bedding Technology violate flammability standards, risking fire injury or death. Consumers must stop using immediately and get a free fire-resistant cover.
KoorlianAug 20, 2026 - Stop using nowConsumer product
JINHEZO Mini Waterproof LED Tea Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Button Cell Batteries; Imported by Mystic ZO
JINHEZO Mini Waterproof LED Tea Lights recalled due to button battery ingestion hazard. Risk of serious injury or death if swallowed. Consumers must stop use and request refund via email with order details.
JINHEZOAug 20, 2026 - Stop using nowConsumer product
Goal Zero Recalls YETI 3000X Power Stations Due to Serious Risk of Injury from Fire and Burn Hazards
Goal Zero recalls YETI 3000X power stations due to overheating circuit boards that pose fire and burn risks. Stop using immediately and install a free firmware update.
Goal ZeroAug 20, 2026 - Stop using nowConsumer product
CCM Hockey U.S. Recalls FMHVR Hybrid Visors and ACCHVR Replacement Visor Accessories Due to Risk of Injury from Laceration or Impact Hazards
CCM recalls FMHVR Hybrid Visors and ACCHVR Replacement Visor Accessories due to risk of laceration or impact injury from cracking upon impact. Return to retailer for free replacement.
CCMAug 20, 2026 - Use cautionMedical device
Cardinal Health 200, LLC recalls Presource Packs containing Medtronic Microstream Components: Intubation Kit Catalog Numbers AN23366084 AN23366085
Cardinal Health recalls 210 Presource Packs containing Medtronic Microstream components due to potential delays in treatment and risk of unintended extubation.
Cardinal HealthAug 19, 2026 - UnratedMedical device
SEASPINE ORTHOPEDICS CORPORATION recalls SeaSpine Mariner Deformity Product Name: Extended Polyaxial Head, Attached Gimbal, 12mm REF: MD1-300010-12
SeaSpine recalls specific Mariner Deformity products due to proximal thread depth being out of design specs. Affected units include model MD1-300010-12 with certain lot numbers. No remedy provided in official notice.
SeaSpineAug 19, 2026 - Lower riskMedical device
Olympus Corporation of the Americas recalls Olympus EZDilate Endoscopic Balloon Dilator Wired-guided 11, 12, 13mm. Model Number: BD-420X-1355.
Olympus recalls EZDilate Endoscopic Balloon Dilators with model BD-420X-1355 due to potential incorrect inflation chart labels that could lead to improper balloon sizing.
OlympusAug 19, 2026 - Use cautionMedical device
Olympus Corporation of the Americas recalls Olympus BiCOAG Hemostasis Probe 7Fr Fixed Pin Connector. Model/Catalog Number: CD-B622LA.
Olympus recalls BiCOAG Hemostasis Probe 7Fr Fixed Pin Connector (CD-B622LA) due to potential ceramic tip detachment from improper adhesive application. All unexpired lots affected.
OlympusAug 19, 2026 - Lower riskFood
United Sugar Producers and Refiners recalls Light Brown Sugar, Packaged in he follow configurations: 1. United, Net Wt. 50 lbs., (22.68kg). Item Number 810051.
United Sugar Producers & Refiners recalls Light Brown Sugar with potential wheat kernel contamination. Affected products include 50-lb bags (Item 810051) and 2-lb packages (Item 817773).
United SugarAug 19, 2026 - Lower riskMedical device
BD SWITZERLAND SARL recalls BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusion Set, 15 Micron Filter,
BD recalls specific Alaris Pump Infusion Sets due to performance data discrepancies that may lead to inappropriate pump function. Affected models include various 0.2 micron filter and SmartSite Y-site sets. No remedy is provided in the recall notice.
BDAug 19, 2026 - Use cautionMedical device
NOXBOX LTD recalls NOxBOXi Nitric Oxide Delivery System.
NOXBOX recalls Nitric Oxide Delivery Systems with potential oxygen tubing leaks that may cause oxygen desaturation. Affected units have specific serial numbers listed in the recall notice.
NOXBOXAug 19, 2026 - Use cautionMedical device
Stryker Sustainability Solutions recalls REF:2B5ST Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/OPTIVIEW TECHNOLOGY & SLEEVE 5MM X 75MM
Stryker recalls XCEL Bladeless Trocar W/Optiview models with specific serial numbers due to potential cracking during use. Affected units may separate, causing injury. Contact Stryker for details.
StrykerAug 19, 2026 - Stop using nowDrug
B BRAUN MEDICAL INC recalls 0.9% Sodium Chloride Injection, USP, 100 mL Partial Fill in 150 mL PAB Container, Sterile, Rx only, B. Braun Medical
B. Braun Medical recalls 100mL sodium chloride injections with particulate matter (iron oxide, cellulose, polystyrene) in specific lots. Stop using if you have these lots.
B. Braun MedicalAug 19, 2026 - Lower riskFood
Panorama Produce Sales Inc. recalls Martina brand Fresh Whole Mangoes; Individual whole mangoes, variable weight; 9 mangoes per carton box
Martina brand Fresh Whole Mangoes may contain Salmonella. Consumers should avoid these mangoes from specific lots to prevent foodborne illness.
MartinaAug 19, 2026 - Lower riskDrug
Chiesi USA, Inc. recalls Revcovi (elapegademase-lvlr) Injection, 2.4mg/1.5mL (1.6 mg/mL), Single-Dose Vial, Rx Only, For Intramuscular Use Only,
Chiesi USA recalls Revcovi injection due to stability issues. The product may not maintain proper protein concentration. Affected units have specific lot numbers and expiration dates.
ChiesiAug 19, 2026 - Lower riskDrug
American Health Packaging recalls Buprenorphine Sublingual Tablets (C-III), 2 mg, 30 Tablets (3x10), Rx only, Distributed by: American Health Packaging,
American Health Packaging recalls 2mg Buprenorphine Sublingual Tablets (C-III) due to labeling mix-up. This may cause confusion with similar products. Check carton NDC 60687-481-21 for affected items.
American Health PackagingAug 19, 2026
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83,609 recalls tracked · 72,041 explained in plain English · 10,977 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.