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 riskFood
AMY'S KITCHEN INC. recalls Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT. 14.5 OZ. (411 g) Microwave: Place soup in a microwave-safe bowl.
Amy's Kitchen recalls organic lentil soup with potential spoilage. Learn about affected products, safety risks, and how to handle this food recall.
Amy's KitchenJun 22, 2026 - Use cautionMedical device
MUNEVO GMBH recalls munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free Control Application/Smart Glasses
Munevo recalls powered wheelchair hands-free control software versions 10.14.5-12.0.4 and 10.17.5-12.0.4 that may cause steering drift or loss of control, risking collisions or injuries.
MunevoJun 19, 2026 - Lower riskMedical device
Boston Scientific Corporation recalls Boston Scientific TheraSphere 360 Y-90 Management Platform, Model Number M00139509001; Radiological Image Processing
Boston Scientific recalls TheraSphere 360 Y-90 Management Platform software versions with a calculation error when modifying inputs after adding vials to cart. Affected units may need correction.
Boston ScientificJun 19, 2026 - Use cautionMedical device
Ferno-Washington Inc recalls Power F2 Powered Fastening System, Product No. 0567091 Powered fastening system intended for professional use only.
Ferno-Washington recalls Power F2 Powered Fastening System (Product No. 0567091) due to potential roller wear and rail deformation that may cause transport delays for patients.
Ferno-WashingtonJun 19, 2026 - Stop using nowFood
General Mills James Ford Bell Technical Center recalls Pillsbury Bread Rolls, Hard Roll Dough. 180 units / 2.25oz each. Net Wt. 25.31 lb (11.48kg) Package UPC 721582-13283 4.
General Mills recalls Pillsbury Bread Rolls and Hard Roll Dough due to potential foreign material (glass). Check your lot numbers and UPCs.
PillsburyJun 19, 2026 - UnratedFood
Fayus Inc. recalls OLA-OLA POUNDED GROUNDNUTS (INTWILO) NET WT. 32 oz., 2 lbs. (0.907 kg) Distributed by: Yusol International Foods
Fayus recalls OLA-OLA Pounded Groundnuts (Intw: 32 oz) due to undeclared peanuts. Consumers should check UPC 650655764330 and lots L536531/L500505 for affected products.
FayusJun 19, 2026 - Use cautionMeat & poultry
Power Plate Meals, LLC Recalls Frozen Meatloaf Products Due to Misbranding and Undeclared Allergens
USDA recalls 5,795 pounds of frozen meatloaf with garlic mashed potatoes due to undeclared soy allergen. Consumers urged not to consume; products should be thrown away or returned.
Power Plate MealsJun 18, 2026 - Stop using nowFood
CAMPO RICO FOODS LLC recalls Kanni Delight 31/40 Fresh Frozen Vannamei White Shrimp IQF, Raw Peeled & Deveined Tail Off, Gross Weight: 5 lb.,
Campo Rico Foods LLC recalls Kanni Delight frozen shrimp due to detected nitrofurans. Check your freezer for affected batches sold in LA.
Campo Rico FoodsJun 18, 2026 - Use cautionVehicle
LEXUS RZ (2026) recall — Electrical System
Toyota is recalling 2026 Lexus RZ vehicles with electrical system faults that may cause loss of drive power, increasing crash risk. Owners will receive free software updates from dealers.
ToyotaJun 18, 2026 - Use cautionVehicle
CADILLAC VISTIQ (2027) recall — Seats
Cadillac Vistiq 2026-2027 vehicles may trap a child when rear seat folds. Owners must contact dealers for free software update by August 6, 2026.
CadillacJun 18, 2026 - Use cautionFood
Provision Health Corp. dba PH Labs recalls Vista MAX; Dietary Supplement, 90 Capsules. Serving Size: 4 Capsules; Distributed by: Vision of Health, Bell, CA 90201
Provision Health Corp. recalls Vista MAX dietary supplement (90 capsules) due to undeclared Yellow #5. Check your lot numbers and expiration dates.
PH LabsJun 18, 2026 - Lower riskFood
MARS SNACKING recalls MorningStar Farms Buffalo Chik'n Nuggets, 100% Plant Protein Vegan Nuggets, Net Wt. 10.5 oz. (298g), packaged in a
Mars Snacking recalls Buffalo Chik'n Nuggets and Vegan Nuggets due to potential plastic contamination. Check packaging for UPC 028989101105 and use by dates up to July 2027.
Mars SnackingJun 18, 2026 - Stop using nowConsumer product
Veseacky Pajama Sets Recalled Due to Risk of Serious Injury Death from Burn Hazard; Violate Mandatory Standards for Children's Sleepwear
Veseacky recalls pajama sets sold to children due to burn hazard violating safety standards. Consumers must stop using and destroy sets by cutting in half, then send photo for refund.
VeseackyJun 18, 2026 - Stop using nowConsumer product
Spa Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violate Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Arrogantf
Arrogantf spa drain covers recalled due to entrapment and drowning hazards. Violate Virginia Graeme Baker Pool & Spa Safety Act. Stop using immediately and return for refund.
ArrogantfJun 18, 2026 - Stop using nowConsumer product
SHEIN Distribution Corporation Recalls Michley Children's Pajamas Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Standard for Children's Sleepwear
SHEIN recalls Michley children's pajamas due to burn hazard. Products sold in green, pink, yellow, and purple with animal patches pose risk of serious injury or death.
SHEINJun 18, 2026 - Stop using nowConsumer product
Joolz Recalls Aer2 Car Seat Adapters for Strollers Due to Risk of Serious Injury or Death from Suffocation and Fall Hazards; Violates Mandatory Standard for Infant Sleep Products
CooCooBaby recalls Classic and Deluxe Baby Loungers due to suffocation and fall hazards. The loungers violate infant sleep safety standards, risking serious injury or death.
CooCooBabyJun 18, 2026 - Stop using nowConsumer product
Joolz Recalls Aer2 Car Seat Adapters for Strollers Due to Risk of Serious Injury from Fall Hazard
Joolz recalls Aer2 Car Seat Adapters for strollers due to risk of serious injury from potential fall hazard. Consumers must stop using immediately and register for refund via provided link.
JoolzJun 18, 2026 - Stop using nowConsumer product
GOPO Toys Recalls Pull String Teething Toys Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys
GOPO recalls pull string teething toys due to small silicone strings that can cause choking. Consumers must stop using immediately and follow destruction steps for refunds.
GOPOJun 18, 2026 - Stop using nowConsumer product
Bada Boom Fireworks Recalls Pyro Diablo "Diablo Rising" Fireworks Due to Risk of Serious Injury or Death from Explosion and Burn Hazards; Violate Fireworks Ban
Bada Boom recalls Pyro Diablo "Diablo Rising" fireworks due to explosion and burn risks from exceeding federal limits. Stop using immediately for refund.
Bada BoomJun 18, 2026 - Stop using nowConsumer product
BABESIDE Doll and Stroller Children's Toys Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violate Small Parts Ban; Sold on Amazon by HYBDOLLS
BABESIDE doll and stroller toys recalled due to small parts choking hazard. Products sold on Amazon by HYBDOLLS. Consumers must stop using and destroy plush bear and pacifier.
BABESIDEJun 18, 2026 - Stop using nowConsumer product
Arizer Solo III Portable Vaporizers Recalled Due to Fire and Burn Hazards; Risk of Serious Injury or Death; Imported by 7111495 Canada
Recalled Arizer Solo III portable vaporizers (black) pose fire and burn hazards. Consumers must stop using immediately and return for a replacement Solo III V2 unit.
ArizerJun 18, 2026 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion under the following System Descriptions and corresponding model numbers: 1. Azurion 3 M12; Model
Philips recalls Azurion 3 M12, M15, 5 M12, 5 M20, 7 B12, 7 B20, 7 M12, and 7 M20 X-ray systems with specific model numbers due to potential loss of imaging functionality from unauthorized hard drives.
PhilipsJun 17, 2026 - Use cautionMedical device
Boston Scientific Neuromodulation Corporation recalls INFINION CX LEAD KIT, 50CM, Model: SC-2317-50, Material: M365SC2317500; INFINION CX LEAD KIT, 70CM, Model: SC-2317-70,
Boston Scientific recalls INFINION CX lead kits (50cm and 70cm models) due to potential lead fractures causing inadequate spinal stimulation. Affected users should contact for repair or replacement.
Boston ScientificJun 17, 2026 - Lower riskMedical device
Freudenberg Medical, LLC recalls Blom-Singer Classic Indwelling Voice Prosthesis, 16Fr/10 mm REF: 1610-LF
Freudenberg Medical recalls Blom-Singer Classic Indwelling Voice Prosthesis (16Fr/10 mm REF: 1610-LF) due to incorrect labeling that could lead to improper use. Affected units have specific lot numbers and UDI codes.
Freudenberg MedicalJun 17, 2026 - UnratedMedical device
Windstone Medical Packaging, Inc. recalls AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Dr Fred Chiu Single Shot Epi Tray - Rx, Part
Windstone Medical Packaging recalls specific AMS medical convenience kits containing Elevaris Lidocaine HCl injection USP due to supplier quality issues. Affected kits include Dr Fred Chiu Single Shot Epi Trays with listed part numbers and lot numbers.
Windstone Medical PackagingJun 17, 2026 - Lower riskMedical device
Paragon 28, Inc. recalls P28 PHANTON INTRAMEDULLARY NAIL SYSTEM, Phantom Hindfoot TTC/TC Ball Tipped Guide Rod, SIZE: 0.30 mm, LENGTH: 800 mmm,
Paragon 28 recalls P28 Phantom Hindfoot Nail System due to potential sterile packaging breaches. Affected units have specific model and lot numbers. Consumers should check their product details and contact the company for guidance.
Paragon 28Jun 17, 2026 - Lower riskMedical device
Medtronic Neurosurgery recalls Ventriculostomy Kit, REF: 46154
Medtronic Neurosurgery recalls Ventriculostomy Kit REF 461: endotoxin levels may exceed safe limits for cerebrospinal fluid contact, causing inflammation. Affected units sold with UDI-DI 00673978947396 and Lot 2025-08779.
Medtr: NeurosurgeryJun 17, 2026 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Perampanel CIII Tablets, 6mg, Rx only, 30 Tablets, Mfd.by: Taro Pharmaceutical Industries Ltd., Haifa Bay, Israel
Sun Pharmaceutical recalls Perampanel CIII 6mg tablets due to label mix-up with 10mg tablets. Affected units contain incorrect labeling that may lead to incorrect dosing.
Sun PharmaceuticalJun 17, 2026 - Lower riskMedical device
BD SWITZERLAND SARL recalls 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 MaxPlus Ext Set w/Needleless and Y-Site
BD recalls 60-inch non-DEHP minibore extension sets with UDI-DI codes 10885403236235, 10885403274619, and 10885403237218 due to potential inadequate sterilization processing.
BDJun 16, 2026 - Lower riskMedical device
Copan WASP recalls Brand Name: WASPLab Product Name: WASPLab Model/Catalog Number: W087 Software Version: WebApp version 2.33.1, 2.33.3
WASPLab W087 devices with WebApp versions 2.33.1, 2.33.3, and 2.34.2 may prevent overwriting results. Consumers should check their software version and contact support for updates.
WASPLabJun 16, 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.