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- Stop using nowConsumer product
Yamazuki Recalls Youth All-Terrain Vehicles (ATVs) Due to Risk of Serious Injury or Death from Crash; Violate Mandatory Standard for ATVs
Yamazuki recalls Sunderwell XW-A17 youth ATVs sold online due to missing brake lights, which create a deadly crash hazard. Stop using immediately.
SunderwellJun 25, 2026 - Stop using nowConsumer product
Super Off-Road Solar Power Banks Recalled Due to Overheating; Imported by Spector & Co.
Super Off-Road 12,000 mAh Solar Wireless Power Banks recalled due to lithium-ion battery overheating and swelling, posing burn risk. Consumers must stop using and return for refund.
Spector & Co.Jun 25, 2026 - Stop using nowConsumer product
Southern Telecom Expands Recall of Lomi Waxing Kits Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Additional Model and Reported Incidents
Southern Telecom recalls Lomi Roll-On Waxing Kits (models LOMB2003PK, LOMB2004PK) due to risk of fire, burns and electrical shock from overheating power cords. Consumers must stop using immediately and destroy kits by cutting power cord and uploading photo to support site.
LomiJun 25, 2026 - Stop using nowConsumer product
Shield Line Recalls MedPride Baby Oil Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging
MedPride Baby Oil bottles lack child-resistant packaging, posing a risk of serious injury or death from child poisoning. Consumers should secure bottles out of reach and contact Shield Line for a refund.
MedPrideJun 25, 2026 - Stop using nowConsumer product
Raychy Children's Light Sneakers Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Coin Batteries; Imported by Carina and Rambo
Raychy Children's Light Sneakers with coin batteries recalled due to ingestion hazard. Stop using immediately to prevent serious injury or death.
RaychyJun 25, 2026 - Stop using nowConsumer product
Montessori Busy Board Toys Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by Small Fish
Small Fish Montessori Busy Board toys (model 2512JX02) recalled due to magnets detaching and causing serious injury or death if swallowed. Consumers must stop using and dispose of items.
Small FishJun 25, 2026 - Stop using nowConsumer product
Kith Retail Recalls Children's Loungewear Sets Due to Risk of Serious Injury from Burn Hazard; Violate Mandatory Standards for Children's Sleepwear
Kith recalls children's lounge sets sold in black/red plaid that violate flammability standards for sleepwear, risking serious burns. Consumers must stop using and destroy items by cutting in half.
KithJun 25, 2026 - Stop using nowConsumer product
Honlyne LED Party Favors Recalled Due to Risk of Serious Injury Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Button Cell Batteries; Sold by Huizhou Rongheng Network Technology
Honlyne LED party favors with button cell batteries recalled due to risk of serious injury or death if swallowed by children. Consumers must stop using and contact for refund.
HonlyneJun 25, 2026 - Stop using nowConsumer product
Daikin Comfort Technologies Manufacturing Recalls Amana Air Conditioners and Heat Pumps Due to Risk of Serious Injury from Fire and Burns
Daikin recalls certain Amana window and through-the-wall air conditioners and heat pumps due to heating element remaining energized after being turned off, risking fire or burns. Affected units have model numbers starting with PB, AH, or AE.
DaikinJun 25, 2026 - Use cautionConsumer product
Combination Smoke and Carbon Monoxide (CO) Detectors Recalled Due to Risk of Serious Injury or Death from Failure to Alert Consumers to Fire; Sold Exclusively on Amazon.com by Treatlife Technology
Treatlife Smoke and CO detectors with FCC ID 2ANDL-XR3, sold on Amazon, recalled due to risk of failing to alert to fire. Consumers must get a replacement and mark recalled units.
TreatlifeJun 25, 2026 - Lower riskMedical device
BioFire Diagnostics, LLC recalls BIOFIRE Respiratory Panel 2.1 (RP2.1) REF 423742 UDI code: 00815381020529 PCR-based multiplexed nucleic acid test, in
BioFire recalls Respiratory Panel 2.1 (RP2.1) REF 423742 due to increased false negative results in PCR tests. Affected units have UDI code 00815381020529.
BioFireJun 24, 2026 - Lower riskMedical device
Covidien, LP recalls Dermalon 88861757-31 DERMALON* 4-0 BLU 75CM C13 88861757-31 88861799-31 DERMALON* 4-0 BLU 75CM C14 88861799-31
Covidien recalls Dermalon 4-0 Blue 75cm sutures with possible packaging tears that could cause infection. Affected items have specific lot numbers and model codes. Consumers should check their product details.
CovidienJun 24, 2026 - Use cautionMedical device
Maquet Critical Care AB recalls Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 Flow-i C20 6888520 Flow-i C30 6888530
Maquet recalls Flow-i C20, C30, and C40 anesthesia machines with specific serial numbers due to risk of insufficient anesthesia delivery during surgery, potentially causing patient awareness.
MaquetJun 24, 2026 - Stop using nowMedical device
Medtronic Perfusion Systems recalls EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR, intended for use with cardiopulmonary bypass as an arterial
Medtronic recalls EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR for possible pinhole leaks during cardiopulmonary bypass that could cause bleeding, vessel damage, or organ failure.
Medtronic Perfusion SystemsJun 24, 2026 - Stop using nowDrug
JB Chemicals and Pharmaceuticals Ltd recalls Cetirizine Hydrochloride Tablets USP 5 mg, 100-count bottle, Manufactured by: Unique Pharmaceuticals Labs, (A Div. of
JB Chemicals recalls 34,020 bottles of Cetirizine Hydrochloride Tablets due to Ranitidine cross-contamination. Check your lot numbers immediately.
JB ChemicalsJun 24, 2026 - Use cautionMedical device
ICU Medical Inc. recalls Hotline Fluid Warming Set, single use device, is designed to warm blood and intravenous fluids and deliver them to the
ICU Medical recalls specific lots of Hotline Fluid Warming Sets due to potential leakage. Affected units may cause fluid leaks during medical use. Contact for details.
ICU MedicalJun 24, 2026 - Use cautionVehicle
HYUNDAI TUCSON HYBRID (2025) recall — Electrical System
Hyundai recalls 2025-2026 Tucson Hybrid vehicles with potential instrument panel display failure, risking critical safety information loss. Owners must update software via OTA or dealer by August 2026.
HyundaiJun 24, 2026 - Use cautionVehicle
FORD BRONCO (2022) recall — Structure
Ford is recalling 2022-2026 Bronco vehicles with potentially detachable fender flares that could increase crash risk. Owners must have fender flares inspected or replaced by dealers at no cost.
FordJun 24, 2026 - Use cautionVehicle
FORD EXPLORER (2020) recall — Power Train
Ford is recalling 2020 Explorer vehicles with potential park system damage causing rollaway and crash risk. Owners must contact Ford for free software update and transmission repair.
FordJun 24, 2026 - UnratedDrug
QuVa Pharma, Inc. recalls Methohexital Sodium, 100 mg/10 mL (10 mg/mL), Total Volume: 10 mL, Rx only, Compounded drug, QuVa Pharma, 1075 W Park
QuVa Pharma recalls specific lots of Methohexital Sodium injection due to failed impurity specifications. Check lot numbers and expiration dates for affected units.
QuVa PharmaJun 24, 2026 - UnratedDrug
Reliance Life Sciences Private Limited recalls Pemetrexed for Injection 500mg/Vial, 1 50 mL Single-Dose Vial per carton, For intravenous use only, Rx only,
Reliance Life Sciences recalls Pemetrexed for Injection 500mg/vial due to lack of sterility assurance. This medication is for IV use only with a prescription. Affected lots expire Jan 2028.
Reliance Life SciencesJun 24, 2026 - Use cautionFood
Lehi Valley Trading Company, Inc recalls High Valley Orchard Chocolate Covered Raisins, net wt. 15oz. per package, each case contains 12/15oz. bags. Product is
High Valley Orchard Chocolate Covered Raisins (15oz) recalled due to unintended undeclared peanut from mis-packaging. Consumers should avoid use to prevent allergic reactions.
High Valley OrchardJun 24, 2026 - Stop using nowFood
Trafa Pharmaceutical Inc. recalls Trafa Pharmaceuticals Inc. brand ORGANIC MORINGA LEAF POWDER; NET WEIGHT: 15 KGS; packaged in brown paper bags with a
Trafa Pharmaceuticals recalls 15kg organic moringa leaf powder with potential Salmonella contamination. Affected batches include brown paper bags with white label and batch #TRF-2025050801. Consumers should check their products for this specific batch.
Trafa PharmaceuticalsJun 24, 2026 - Lower riskFood
Bear Stewart Co recalls Bakr Brown Butter Chocolate Chunk Ready to Bake Cookie Dough, 8-oz pouch 12 cookies per pouch, UPC 8 50073 08700 8, 8
Bear Stewart Co recalls 8-oz chocolate cookie dough pouches with undeclared soy. Consumers should check UPC 8 50073 08700 8 for affected products.
Bear Stewart CoJun 24, 2026 - Lower riskMedical device
Arrowhead DE LLC recalls Arrow-LOK Implant, REF: 21-253519, 21-253522, 21-253525, 21-253528, 21-253530, 21-253533, 21-253535, 21-253540,
Arrowhead DE LLC recalls Arrow-LOK Implant due to potential reduction in sterility assurance, which could lead to patient infection. Affected units include specific reference numbers.
ArrowheadJun 23, 2026 - Stop using nowMedical device
Therabody, Inc recalls Charger for the Therabody Theragun, G4 PRO massage device, and products which include the 4th Generation Theragun PRO
Therabody recalls G4 PRO charger for fire risk due to overheating during charging. Affected units include specific models sold in 2022 and earlier. Stop using immediately to prevent fire.
TherabodyJun 23, 2026 - Lower riskDrug
Padagis US LLC recalls Nystatin Cream USP, (100,000 USP Nystatin Units), NET WT 15 g, Rx only, 15 g tube, Manufactured by Padagis, Yeruham,
Padagis recalls 15g Nystatin Cream USP (Rx only) due to low drug potency from stability testing. Consumers should contact manufacturer for details.
PadagisJun 23, 2026 - Lower riskDrug
Lupin Pharmaceuticals Inc. recalls Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection USP, 1mg per vial, Diluent for Glucagon, 1 mL
Lupin Pharmaceuticals recalls Glucagon Emergency Kits due to a CGMP deviation in stability testing. Affected kits have specific lot numbers and expiration dates. Consumers should contact the manufacturer for details.
LupinJun 23, 2026 - Use cautionVehicle
FOREST RIVER RPOD (2025) recall — Electrical System
Forest River recalls certain 2025-2026 RPOD recreational trailers due to potential electrical shock from mislabeled 110V circuits. Owners should contact customer service for free circuit label replacement.
Forest RiverJun 22, 2026 - UnratedDrug
Direct Rx recalls DULOXETINE D/R, a) 30 mg (NDC 61919-482-30), 30 Caps; b) 30 mg (NDC 61919-482-60), 60 Caps; CYMBALTA, Packaged and
Direct Rx recalls DULOXETINE D/R 30mg capsules (NDC 61919-482-30) and 60-capsule packs (NDC 61919-482-60) due to N-nitroso-duloxetine impurity exceeding FDA safety limits. Affected lots expire 04/30/2027.
Direct RxJun 22, 2026
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