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 cautionMeat & poultry
Stuffed Foods LLC Recalls Frozen Snack Products Due to Misbranding and an Undeclared Allergen
Stuffed Foods LLC recalls 1,818 pounds of frozen Mac & Cheese Bites for containing undeclared soy, a known allergen, which may cause allergic reactions. Consumers are urged not to consume these products.
Stuffed Foods LLCNov 11, 2020 - Lower riskMedical device
RAYSEARCH LABORATORIES AB recalls RayStation 4, 4.5, 4.7, 4.9, 5, 6, 7, 8A, 8B, 9A, 9B, RayPlan 1, 2, 7, 8A, 8B, 9A, 9B, including all service packs.
RaySearch recalls specific versions of RayStation and RayPlan software due to potential incorrect treatment plan reports, which could affect radiation therapy accuracy. Affected users should check their software versions.
RaySearchNov 11, 2020 - Lower riskMedical device
WELCH ALLYN, INC/MORTARA recalls ELI 380 Electrocardiograph - Product Usage: intended to be a high-performance, multichannel resting electrocardiograph.
Welch Allyn recalls ELI 380 electrocardiographs due to potential wireless disconnection from access points, which may disrupt medical monitoring. Affected units have specific part numbers listed in the recall notice.
Welch AllynNov 11, 2020 - Lower riskMedical device
Canon Medical System, USA, INC. recalls Canon PET-CT SCANNER, Cartesion Prime, MODEL PCD-1000A
Canon Medical recalls PET-CT scanner model PCD-1000A due to software causing potential rescanning and contrast reinjection. Affected units have specific serial numbers.
Canon MedicalNov 11, 2020 - Lower riskMedical device
Intersurgical Inc recalls Smoothbore breathing system with exhalation port 22 mm Device REF #: B0062001 Custom Anasthesia Breathing Systems;
Intersurgical recalls Smoothbore breathing systems with incorrect 22mm exhalation port (model B0062001) due to gas leakage risk during anesthesia. Affected units include lot numbers 4200283 and 4200286.
IntersurgicalNov 11, 2020 - Use cautionMedical device
Westmed, Inc. recalls REF 0562, Adult Elongated O2/CO2 Mask, 10'X0.50 GSL w/ Swivel Elbow, 2" Pigtail w/Female Luer Connectors, 7' Oxygen
Westmed recalls adult oxygen/CO2 masks with potential loose connections causing delayed treatment. Affected units have specific model and lot numbers.
WestmedNov 11, 2020 - UnratedMedical device
Terumo Cardiovascular Systems Corporation recalls (1) Capiox FX25 (West) Advance Oxygenator- with left port, 4-liter Reservoir, XC modified to Advance, Sterile Catalog
Terumo recalls Capiox FX25 Advance Oxygenators with incorrect East/West configuration for heart surgery. This may cause improper gas exchange during cardiopulmonary bypass. Affected units have specific catalog numbers and lot numbers.
TerumoNov 11, 2020 - Lower riskMedical device
Integra LifeSciences Corp. recalls Instruction Manual for Mayfield A2000 Skull Cap - Product Usage: intended for or rigid skeletal fixation during
Integra LifeSciences recalls revised instruction manuals for Mayfield A2000 skull cap. The update corrects illustrations for neurosurgical use to ensure safe rigid skeletal fixation.
Integra LifeSciencesNov 11, 2020 - Lower riskDrug
InvaTech Pharma Solutions, LLC recalls Levocetirizine Dihydrochloride Tablets, USP, 5 mg 30-count bottle, Rx Only, Distributed by: Marlex Pharmceuticals, Inc.
InvaTech Pharma Solutions recalls 5mg Levocetirizine tablets that failed stability testing. Affected lots may degrade, causing potential safety issues. Contact for details.
InvaTech Pharma SolutionsNov 11, 2020 - Lower riskDrug
Teva Pharmaceuticals USA recalls Testosterone Gel 1%, 2.5 grams per unit dose, packaged in 2.5 gram Unit-Dose Packets (NDC 0591-3216-17); 30 Unit-Dose
Teva Pharmaceuticals USA recalls Testosterone Gel 1% (2.5g units) due to high drug concentration in stability testing. This may cause unsafe levels of testosterone. Contact for details.
Teva Pharmaceuticals USANov 11, 2020 - Lower riskDrug
Apotex Corp. recalls Aripiprazole Tablets, USP 15 mg tablets, packaged in a) 1000 count bottle, NDC 60505-2675-8; b) 30 count bottle, NDC
Apotex recalls 15mg Aripiprazole tablets that failed dissolution tests. These prescription-only pills may not release medication properly. Consumers should contact Apotex for details.
ApotexNov 11, 2020 - Lower riskMedical device
Applied Medical Technology Inc recalls AMT Male ENFit-to-Stepped Male (Christmas Tree) Adapter, Model Number ETRN102. Box PN TRN102, Box UDI
Applied Medical Technology recalls AMT Male ENFit-to-Stepped Male adapters with incorrect pouch labels. Consumers should check labels to avoid using faulty products.
Applied Medical TechnologyNov 10, 2020 - Lower riskMedical device
Baxter Healthcare Corporation recalls MiniCap Extended Life PD Transfer Set
Baxter Healthcare recalls MiniCap Extended Life PD Transfer Sets with potential no-flow and leaks under twist clamp. Affected units have specific product codes and expiration dates. Contact Baxter for details.
Baxter HealthcareNov 10, 2020 - UnratedMedical device
CryoLife, Inc. recalls CryoValve SG Pulmonary Human Heart Valve. The valve is cryopreserved in a tissue culture medium containing
CryoLife recalls SG Pulmonary Heart Valves with microbial culture test failures in processing. Affected units have specific serial numbers and UDI codes. Consumers should contact CryoLife for details.
CryoLifeNov 10, 2020 - Lower riskMedical device
TissueTech, Inc. recalls PROKERA Plus, non-sterile - Product Usage: Biologic corneal bandage.
TissueTech recalls non-sterile PROKERA Plus corneal bandages due to potential microbial contamination. Affected lots and serial numbers listed. Consumers should contact TissueTech for details.
TissueTechNov 10, 2020 - Lower riskMedical device
Merit Medical Systems, Inc. recalls Product Code: K05T-02533, Custom Inflation Kit, Custom K05 Sterile EO, Rx Only, (01)00884450255803 For
Merit Medical recalls custom angiography kits due to potential non-sterile devices causing infections. Affected kits may have compromised sterile barriers. Consumers should contact Merit Medical for details.
Merit Medical SystemsNov 10, 2020 - Lower riskDrug
EYWA PHARMA INC recalls Levetiracetam Tablets, USP 500 mg, packaged in 120-count bottle, Rx only, Manufactured by: VKT Pharma Private Limited
EYWA Pharma recalls 500mg Levetiracetam tablets due to foreign 1000mg tablets found in some 120-count bottles. Affected products contain specific lot numbers and manufacturing dates.
EYWA PharmaNov 10, 2020 - Lower riskFood
High Quality Organics recalls HQO High Quality Organics Organic Thyme Leaves, Whole Net Weight 30 lbs., 500 lbs. High Quality Organics 1201 Moya
High Quality Organics recalls organic thyme leaves due to potential Salmonella contamination. Affected lots include 48040 with best by date 2022-10-30. Consumers should check labels and contact the company for details.
High Quality OrganicsNov 10, 2020 - Use cautionConsumer product
Ring Recalls Video Doorbells (2nd Generation) Due to Fire Hazard
Ring recalls 2nd Gen video doorbells with fire risk if incorrect screws are used during installation. Check your model via serial number on Ring's website to see if you're affected.
RingNov 10, 2020 - Stop using nowConsumer product
Quality Bicycle Products Recalls Salsa Cycles Cutthroat Bicycles Due To Injury Hazard
Recalled 2020 Salsa Cutthroat bicycles with forks containing serial number starting with 'G' may crack, causing falls. Stop using immediately and get free fork replacement.
SalsaNov 10, 2020 - Stop using nowConsumer product
Kohl's Recalls Three-Wick SONOMA Goods For Life Branded Candles Due to Fire and Burn Hazards
Kohl's recalls SONOMA Goods For Life three-wick candles due to fire and burn risks from high flames igniting wax or breaking glass containers. Return to store for refund or credit.
SONOMA Goods For LifeNov 10, 2020 - Stop using nowConsumer product
Fire Pit Tables Sold Exclusively at Big Lots Recalled Due to Fire Hazard; Manufactured by Sunjoy
Sunjoy's Oakmont LP fire pit tables sold at Big Lots recalled due to fire hazard from melted and igniting burner kit hose. Consumers must stop using and get free replacement kit.
SunjoyNov 10, 2020 - Use cautionConsumer product
Bolek's Craft Supplys Recalls Wintergreen Essential Oil Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning
Bolek's Craft Supplys recalls Crafty Bubbles Wintergreen Essential Oil due to non-child-resistant packaging, posing poisoning risk for young children. Consumers should store out of reach and get a refund.
Bolek's Craft SupplysNov 10, 2020 - Stop using nowConsumer product
Arena North America Recalls Swim Snorkels Due to Choking Hazard
Arena recalls Swim Snorkel Pro II and II models due to choking hazard from excess material inside tubes. Consumers must stop using and get free replacements.
ArenaNov 10, 2020 - Use cautionVehicle
FOREST RIVER VENGEANCE (2016) recall — Equipment
Forest River recalls 2014-2016 Vengeance trailers with incorrect water placard causing overload risk. Owners must get free placard update to comply with safety standards.
Forest RiverNov 9, 2020 - Use cautionVehicle
NISSAN TITAN (2019) recall — Exterior Lighting
Nissan is recalling 2019 Titan vehicles with LED headlights that may have incorrect aiming marks, causing insufficient nighttime road illumination and increasing crash risk. Owners should contact Nissan for free headlight assembly replacement.
NissanNov 9, 2020 - Stop using nowVehicle
ISUZU FTR (2020) recall — Electrical System
Isuzu recalls certain FTR and Chevrolet 6500XD vehicles due to a broken ground cable that may cause the power steering hose to rupture and increase fire risk.
IsuzuNov 9, 2020 - Lower riskMedical device
Canon Medical System, USA, INC. recalls Canon Aquilion Prime SP, Multislice Helical CT Scanner, TSX-303B/8L - Product Usage: intended to acquire and display
Canon recalls Aquilion Prime SP CT scanners with serial numbers listed for a software problem that may cause scans to fail, requiring rescanning and contrast reinjection.
CanonNov 9, 2020 - Lower riskMedical device
Helena Laboratories, Corp. recalls K-ACT Actalyke Clotting Test Tubes that are used in the: ACTALYKE XL ACTIVATED CLOTTING TIME ANALYZER, and ACTALYKE
Helena Laboratories recalls K-ACT Actaly: Cracked test tube caps may cause leaks or contamination during blood tests. Affected lots 1-19-K-ACT and 2-19-K-ACT.
Helena LaboratoriesNov 9, 2020 - Lower riskMedical device
ICU Medical, Inc. recalls icumedical Cogent" Hemodynamic Monitoring System - Product Usage: intended for patients for whom the monitoring of
ICU Medical recalls Cogent Hemodynamic Monitoring System due to potential software issue causing incorrect continuous cardiac output readings after PulseCO calibration. Affected units may display wrong cardiac output values.
ICU MedicalNov 9, 2020
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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.