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
IC BUS CESB (2025) recall — Structure
International recalls 2025-2027 IC Bus CESB school buses due to potential body panel separation in crashes, increasing injury risk. Owners must contact customer service for free rivet installation.
InternationalJul 17, 2026 - Stop using nowVehicle
INTERNATIONAL MV (2025) recall — Electrical System
International recalls certain MV and HV vehicles due to a short circuit risk in the battery interconnect cable that may cause a fire. Free dealer repair available.
InternationalJul 17, 2026 - Stop using nowMedical device
Tandem Diabetes Care, Inc. recalls Brand Name: Tandem t:slim mobile application Product Name: t:slim Mobile Application, iOS Model/Catalog Number: iOS
Tandem recalls iOS app v2.13 beta due to pairing failures with Abbott FreeStyle Libre 3 Plus sensors, risking glucose monitoring errors.
Tandem Diabetes CareJul 16, 2026 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion Rystem, Model Numbers: 722063, 722064, 722067, 722068, 722078, 722079, 722221, 722222,722223, 722224,
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. is a leading manufacturer of medical imaging equipment and solutions.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Jul 16, 2026 - Lower riskMedical device
Straumann USA LLC recalls Straumann Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim (Article 021.5314); implant,
Straumann recalls certain Bone Level Tapered implants that may be 12mm instead of 14mm. This could cause improper fit and complications during dental surgery. Affected implants have specific model numbers and lot codes.
StraumannJul 16, 2026 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion, Model Numbers: 722229, 722230, 722231, 722232, 722233, 722234, 722235, and 722236, with Software
PHILIPS
PHILIPSJul 16, 2026 - Lower riskMedical device
Biofire Defense recalls FilmArray NGDS Warrior Panel REF NGDS-ASY-0007 UDI-DI code: (01)00851458005136 The FilmArray NGDS Warrior Panel is a
Biofire Defense recalls FilmArray NGDS Warrior Panel REF NGDS-ASY-0007 with UDI-DI code (01)00851458005136 due to potential outbreak strain mismatch. Affected units may not detect certain pathogens accurately.
Biofire DefenseJul 16, 2026 - UnratedDrug
Central Admixture Pharmacy Services Inc recalls Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag, (patient specific), Compound Volume 416.8 mL per bag,
Central Admixture Pharmacy Services recalls pediatric TPN bags with incorrect formulation. Patients may face health risks from improper nutrition mixtures. Contact for details.
Central Admixture Pharmacy ServicesJul 16, 2026 - UnratedDrug
Ascend Laboratories, LLC recalls Dabigatran Etexilate Capsules, 75 mg, 60-count (6x10)blister pack further packaged in a carton, Rx only, Manufactured
Ascend Laboratories recalls 75mg Dabigatran Etexilate capsules (NDC 0904-7253-68) due to failed impurity tests. This could affect drug safety for patients using blood thinners.
Ascend LaboratoriesJul 16, 2026 - Lower riskFood
CHEER PACK recalls Flexible food pouch (3-layer foil, spouted, #CP6088), manufactured for packaging Pumpkin Tree Peter Rabbit Organics
Cheer Pack recalls flexible food pouches (3-layer foil, spouted, #CP6088) manufactured for Pumpkin Tree Peter Rabbit Organics products due to potential plastic strip release into food. Affected items sold between Oct 25-31, 2025.
Cheer PackJul 16, 2026 - Lower riskDrug
Fresenius Kabi USA, LLC recalls Glycopyrrolate Injection, USP, 1 mg per 5 mL (0.2 mg per mL), 25 x 5 mL fill in a 6.5 mL vial, Rx only, Multiple Dose
Fresenius Kabi recalls Glycopyrrolate injection vials with hair particles. This may cause allergic reactions or other issues. Stop using and contact your doctor.
Fresenius KabiJul 16, 2026 - Use cautionVehicle
JEEP GLADIATOR (2026) recall — Wheels
Chrysler recalls certain 2026 Jeep Gladiator vehicles due to thin steel wheels that may crack or detach, causing loss of vehicle control. Owners must have wheels inspected and replaced by dealers.
ChryslerJul 16, 2026 - Use cautionVehicle
LAND ROVER DISCOVERY (2021) recall — Back Over Prevention
Land Rover is recalling 2021-2025 Discovery vehicles with rearview camera drainage issues that could cause camera damage and reduce driver visibility.
Land RoverJul 16, 2026 - Use cautionVehicle
INFINITI QX80 (2025) recall — Equipment
Nissan recalls certain 2020-2027 QX80 vehicles with incorrect Gross Axle Weight Rating labels that could lead to vehicle overload and crash risk. Owners will receive free label replacements and interim safety notices.
NissanJul 16, 2026 - Stop using nowConsumer product

Warren James Recalls the Copper Cup Found in Flashgitz Relic Lunch Boxes Due to Risk of Serious Injury or Death from Lead Poisoning
Warren James recalls copper cups from Space King No Girls Allowed Relic Lunch Boxes due to lead poisoning risk. Consumers must stop using the cups immediately and contact for replacement.
Warren JamesJul 16, 2026 - Stop using nowConsumer product

Wade Logan Annyka 9-Drawer Fabric Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Imported by Ningbo Jiangdong Peter International Trading
Wade Logan Annyka 9-Drawer Fabric Dressers recalled due to tip-over and entrapment hazards that could cause serious injury or death to children. Unanchored units must be moved away from children.
Wade Logan AnnykaJul 16, 2026 - Stop using nowConsumer product

TOMY Recalls Boon PIVOT Collapsible Toddler Tower Kitchen Step Stools Due to Risk of Serious Injury and Death from Tip-Over and Fall Hazards
TOMY recalls Boon PIVOT Toddler Towers that can tip over, causing serious injury or death. Consumers must stop using immediately and contact TOMY for free repair parts.
TOMYJul 16, 2026 - Stop using nowConsumer product

Target Recalls Cat & Jack Children's Sandals Due to Risk of Serious Injury or Death from Choking Hazard
Target recalls Cat & Jack children's sandals (sizes 5T-12T) due to decorative pearls that can detach and cause choking. Consumers must stop using immediately and return for refund.
Cat & JackJul 16, 2026 - Stop using nowConsumer product

SDADI Kitchen Step Stools Recalled Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards; Imported by Yiwushi Bihe Trading
SDADI wooden step stools (models LT01, LT05) recalled due to tip-over and entrapment risks. Stop using immediately and contact seller for a refund.
SDADIJul 16, 2026 - Stop using nowConsumer product

Panasonic Recalls Electric Toaster Ovens Due to Shock and Fire Hazards
Panasonic recalls all Electric Toaster Ovens (Model NB-G2: stainless steel, 250-500°F) due to risk of shock/fire from insufficient power cord insulation. Consumers must stop using immediately and get a refund.
PanasonicJul 16, 2026 - Stop using nowConsumer product

Oitnlaughter Projecting Finger Light Toys Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by Delightmi
Oitnlaughter LED Finger Lights recalled due to button cell batteries that can cause serious injury or death if swallowed by children. Consumers must stop using and dispose of toys safely.
OitnlaughterJul 16, 2026 - Stop using nowConsumer product

Noerishia Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Hurzein
Noerishia adult portable bed rails (model KDB-504B) recalled due to entrapment and asphyxiation risks. Consumers must stop using immediately and return for refund.
NoerishiaJul 16, 2026 - Stop using nowConsumer product

MNIENT Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails
MNIENT model LQX-110055 bed rails recalled for entrapment, fall, and laceration hazards. Stop using immediately and contact seller for refund.
MNIENTJul 16, 2026 - Stop using nowConsumer product

Madewell Recalls Women's Sweaters Due to Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Standard for Clothing Textiles
Madewell recalls women's sweaters with style numbers NT611 or NT612 that violate textile safety standards, posing a risk of serious burns or death. Consumers must stop using and destroy the sweaters by cutting in half.
MadewellJul 16, 2026 - Use cautionConsumer product

Liizousuda Paint Thinner Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging; Sold on Amazon.com by Shenzhen Gudebo Technology
Liizousuda paint thinner bottles not child-resistant, posing serious poisoning risk for young children. Recalled due to violation of Poison Prevention Packaging Act. Consumers should secure bottles away from children and contact manufacturer for replacement.
LiizousudaJul 16, 2026 - Stop using nowConsumer product

Jobon Torch Lighters Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Violate Mandatory Standard for Multipurpose Lighters
Jobon butane torch lighters recalled due to lack of child-resistant mechanisms causing fire and burn hazards. Consumers must stop using immediately and return for refund.
JobonJul 16, 2026 - Stop using nowConsumer product

Huish Outdoors Recalls Hollis Diving Regulators Due to Risk of Serious Injury or Death from Drowning
Huish recalls Hollis 200LX diving regulators due to cracked inlet tubes causing drowning risk. Stop using immediately and return for free repair.
HuishJul 16, 2026 - Stop using nowConsumer product

Currey & Company Recalls Nottaway Chandeliers Due to Risk of Serious Injury or Death from Electrocution Hazard
Currey & Company recalls Nottaway chandeliers due to lack of electrical grounding, risking electrocution. Consumers must stop using immediately and get a free replacement with installation.
Currey & CompanyJul 16, 2026 - UnratedMedical device
F & A Foundation recalls Reign Medical Clench Staple System (Compression), Description/REF: 9mm x 7mm/152-30907; 11mm x 10mm/152-31110; 15mm x
F & A Foundation recalls Reign Medical Clench Staple Systems (compression) due to unverified bone fixation safety. Affected models include 9mm x 7mm, 11mm x 10mm, and others with specific lot numbers. No remedy specified in recall notice.
F & A FoundationJul 15, 2026 - Lower riskMedical device
Beckman Coulter Inc. recalls Beckman Coulter DxC 500i Clinical Analyzer Modules using software version 1.5 or lower: 1) DxC 500 AU Module w/ISE, DxC
Beckman Coulter recalls DxC 500i Clinical Analyzer Modules with software version 1.5 or lower that may generate incorrect patient test results when importing new Parameter Packages.
Beckman CoulterJul 15, 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.