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- Lower riskMedical device
Medline Industries, LP recalls Medline medical convenience kit labeled as: TRACH TUBE KIT, Medline Kit SKU DYKM2330
Medline recalls medical convenience kit TRACH TUBE KIT (SKU DYKM2330) due to labeling discrepancy. Affected units have specific UDI/DI and lot numbers. No remedy stated in official notice.
MedlineJul 10, 2026 - Lower riskMedical device
AVID Medical, Inc. recalls Halyard LAVH PACK, Model/Catalog Number: USAR053-11 containing Clearify Visualization System (5303907).
AVID Medical recalls Halyard LAVH PACK Model USAR053-11 with Clearify Visualization System (5303907) due to potential leakage after EO sterilization. Affected units have specific UDI/DI and lot numbers.
AVID MedicalJul 10, 2026 - UnratedMedical device
Medline Industries, LP recalls Medline convenience kits labeled as: 1) LAMI FUSION, Medline Kit SKU CDS982035Y; 2) NON MB MJR NEURO CRANI SM PK,
Medline recalls several convenience kits with potentially contaminated components. Consumers should check product labels for specific SKUs and lot numbers to determine if their kit is affected.
MedlineJul 10, 2026 - Use cautionMedical device
GE Medical Systems Information Technologies Inc recalls GE Healthcare Portrait Core Services SW V 1.2.0, REF 5700592. patient monitoring system
GE Healthcare recalls patient monitoring software version 1.2.0 (REF 5700592) due to a software vulnerability that could allow unauthorized access to patient data and monitoring systems.
GE HealthcareJul 10, 2026 - Lower riskMedical device
Medical Action Industries, Inc. 306 recalls Generic Name: Kit, Urine, Clean Catch Trade Name: Kit: Urinary Clean Catch 20/cs Model/Catalog Number: 76769 Lot
Medical Action Industries recalls 4,000 units of Urinary Clean Catch Kit (Lot 333606) with an incorrect expiration date of March 31, 2027 instead of February 28, 2027.
Medical Action IndustriesJul 9, 2026 - Lower riskMedical device
Henry Schein Inc. recalls Grandio Universal Nano-Hybrid Restorative Material - Capsules 0.25Gm, Product Codes: 1) 949-3594, Mfr Product Code
Henry Schein recalls specific Grandio Universal Nano-Hybrid Restorative Material capsules due to incorrect packaging and instructions from FDA-cleared devices. Affected lots include 949-3594 to 949-3597 with listed lot numbers.
Henry ScheinJul 9, 2026 - Lower riskMedical device
AVID Medical, Inc. recalls Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
AVID Medical recalls Halyard TOTAL JOINT Model MSBM036-03 due to latex in statlock component. Affected units may cause allergic reactions. Contact for remedy.
AVID MedicalJul 9, 2026 - Use cautionMedical device
Boston Scientific Corporation recalls Boston Scientific ENROUTE Transcarotid Neuroprotection System Plus, Material Number SR-250-NPS; Percutaneous catheter
Boston Scientific recalls ENROUTE Transcarotid Neuroprotection System Plus (Material Number SR-250-NPS) due to potential arterial sheath tip separation during use. Affected units include specific lot numbers and GTIN.
Boston ScientificJul 9, 2026 - Lower riskFood
Pack'n Fresh LLC recalls "***Hondashi 0.25oz***" seasoning packed in silver plastic/metallic pouch, pouches packed in brown paperboard cartons
Pack'n Fresh recalls 600-pack Hondashi seasoning pouches due to missing fish allergen in labeling. Consumers should check product labels for correct allergen information.
Pack'n FreshJul 9, 2026 - Use cautionVehicle
VOLVO VNL (4) (2026) recall — Steering
Volvo recalls 2026 VNL trucks with loose steering arms that may cause loss of steering control. Owners must have steering inspected by dealers free of charge.
VolvoJul 9, 2026 - Stop using nowVehicle
PETERBILT 579 (2026) recall — Service Brakes, Air
PACCAR recalls certain 2026-2027 Peterbilt 579 tractors due to an incorrectly installed air brake quick release valve that may cause trailer instability.
PeterbiltJul 9, 2026 - Lower riskDrug
CareFusion 213, LLC recalls BD ChloraPrep Clear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol), 60 x 1 mL
BD recalls 60x1mL ChloraPrep Clear antiseptic solution due to potential packaging seal issues that could lead to contamination. Affected lots expire through 2029.
BDJul 9, 2026 - Stop using nowConsumer product
WonderStone Infant Walkers Recalled Due to Risk of Serious Injury or Death from Fall Hazard; Violate Mandatory Standard for Infant Walkers; Sold on Walmart.com by Wonder Stone Toys
WonderStone infant walkers sold on Walmart.com are recalled due to fall hazards. Stop using immediately and contact the manufacturer for a refund.
WonderStoneJul 9, 2026 - Stop using nowConsumer product
Moodooy Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Yuezhang
Moodooy adult portable bed rails (model F311) recalled due to entrapment and asphyxiation risks. Consumers must stop using immediately and contact Yuezhang for refund.
MoodooyJul 9, 2026 - Stop using nowConsumer product
Greenworks Tools Recalls 24V and 48V Kobalt Yard Power Tools with USB-C Batteries Due to Risk of Serious Injury from Fire Hazard
Greenworks/Kobalt recalls yard power tools and batteries with USB-C ports due to fire hazard. Stop charging immediately. Get a free replacement.
KobaltJul 9, 2026 - Stop using nowConsumer product
Flaunt Recalls Magsafe Battery Chargers Due to Risk of Serious Injury or Death from Fire and Burn Hazards
Flaunt recalls MagSafe Battery Chargers with model E33A due to fire and burn hazards from overheating lithium-ion batteries. Consumers must stop using immediately and return for refund or store credit.
FlauntJul 9, 2026 - Stop using nowConsumer product
Conair Recalls Cuisinart Propel+ Four Burner 3-In-1 Gas Grills Due to Risk of Serious Injury from Laceration Hazard
Conair recalls Cuisinart Propel+ Four Burner 3-in-1 Gas Grills with tempered glass pizza oven that can shatter, causing serious laceration injuries. Affected owners should stop using immediately and follow refund steps.
ConairJul 9, 2026 - Stop using nowConsumer product
Biometric Gun Safes Recalled Due to Serious Injury Hazard and Risk of Death; Sold Exclusively on Amazon.com by BBRKIN
BBRKIN and MouTec biometric firearm safes with model QHXP029B recalled due to unauthorized access risk. Stop using biometric feature, remove batteries, and use key only. Contact for free repair kit.
BBRKINJul 9, 2026 - Stop using nowConsumer product
Best Buy Recalls Insignia® Gas Ranges Due to Risk of Serious Injury from a Fire Hazard
Best Buy recalls Insignia gas ranges with model NS-RGFGSS1 and NS-RGFCGS2 due to risk of fire from accidentally activated front knobs. Consumers must stop using and get free knob covers.
InsigniaJul 9, 2026 - Use cautionVehicle
FOREST RIVER WILDWOOD (2027) recall — Equipment
Forest River recalls certain 2026-2027 Wildwood travel trailers due to potential incorrect Gross Vehicle Weight Rating labels, which could lead to vehicle overloading and crash risks. Owners must contact customer service for free label correction.
Forest RiverJul 8, 2026 - Use cautionMedical device
Tobii Dynavox Llc recalls TD Navio Maxi Speech Generating Device Model/Catalog Number: 1000799
Tobii Dynavox recalls TD Navio Maxi speech devices with model 1000799 due to potential battery short circuits causing heat and gas. Affected units have specific serial numbers and were sold from 2024 to 2026.
Tobii DynavoxJul 8, 2026 - Use cautionMedical device
Fort Defiance Industries, LLC recalls Fort Defiance Industries (FDI), Automated Field Steam Sterilizer REF: P2131
Fort Defiance Industries recalls Automated Field Steam Sterilizers REF P2131 due to potential ground connection failure. Affected units may have unreliable fault current return, risking electrical hazards.
Fort Defiance IndustriesJul 8, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline medical convenience kits, labeled as: 1) NEURO CDS, Medline Kit SKU CDS985246J; 2) NEURO PACK, Medline Kit SKU
Medline recalls specific neurosponge kits due to possible endotoxin levels exceeding specifications. Affected kits include NEURO CDS, NEURO PACK, and other medical convenience kits with listed SKUs and lot numbers.
MedlineJul 8, 2026 - Lower riskDrug
Ascend Laboratories, LLC recalls Amlodipine and Olmesartan Medoxomil Tablets, 10 mg/20 mg, 30 Tablets per bottle, Rx Only, Manufactured by: Alkem
Ascend Laboratories recalls 10mg/20mg Amlodipine and Olmesartan Medoxomil tablets (NDC 67877-500-30) due to failed dissolution specs causing low drug content. Rx only, manufactured in India, distributed in US.
Ascend LaboratoriesJul 8, 2026 - Lower riskFood
Man Fon, Inc. recalls Wonton Wrappers packed into clear flexible plastic bag and sold as 40 units (16oz bags)/case. Wonton Wrappers packed
Man Fon recalls wonton wrappers sold in clear plastic bags without ingredient labels, containing undeclared wheat and food dyes. Consumers should check for missing labeling and contact the company for details.
Man FonJul 8, 2026 - Lower riskFood
Green Jeeva LLC recalls Organic Moringa Powder; 15kg/bag (bulk); Product code: GJ96
Green Jeeva LLC recalls 15kg bulk Organic Moringa Powder (product code GJ96) due to salmonella contamination. Consumers should avoid use until notified.
Green JeevaJul 8, 2026 - Use cautionVehicle
TOYOTA GRAND HIGHLANDER (2026) recall — Power Train
Toyota is recalling certain 2026 Grand Highlander models due to potential rear axle carrier failure causing sudden loss of stability and control. Owners must have their rear axle carriers inspected and replaced if necessary at no cost.
ToyotaJul 8, 2026 - Use cautionVehicle
SUBARU FORESTER (2025) recall — Equipment
Subaru recalls 2025 Forester models with incorrect Gross Axle Weight Rating labels that could cause vehicle overload and crash risk. Owners will receive free label updates to comply with safety standards.
SubaruJul 8, 2026 - Use cautionVehicle
TESLA MODEL Y (2026) recall — Structure
Tesla is recalling certain 2026 Model Y vehicles that may lack knee airbags and safety features, increasing crash injury risk. Owners must return vehicles for free repurchase by September 5, 2026.
TeslaJul 7, 2026 - Stop using nowMedical device
INTEGRATED MEDCRAFT LLC recalls Kingfisher Compact Individual First Aid Kit. REF Number: 76656. Containing the affected One-piece Guedel airway
Medcraft recalls Kingfisher Compact First Aid Kits with potentially occluded Guedel airway tips. Affected kits may cause breathing difficulties during emergencies. Stop using immediately if you own the recalled models.
MedcraftJul 7, 2026
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