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
35,069 found- Use cautionConsumer product
Viking Range Recalls Freestanding Gas Ranges Due to Risk of Gas Leak and Fire Hazard
Viking recalls 5 Series Freestanding Gas Ranges (2021 models) due to gas tubing separation causing leaks and fire hazards when burners are used. Consumers must stop using bake/broil/griddle functions and contact Viking for free repairs.
VikingFeb 16, 2022 - Stop using nowConsumer product
Valco Baby Recalls Snap Duo Trend Strollers Due to Fall Hazard
Valco Baby recalls Snap Duo Trend strollers due to front wheels breaking off. Stop using immediately and contact Valco Baby for a free replacement wheel assembly.
Valco BabyFeb 16, 2022 - Stop using nowConsumer product
In-Things Recalls Scarves Due to Violation of Federal Flammability Standard and Burn Hazard; Sold Exclusively at Saksoff5th.com
In-Things recalls 100% sheer silk scarves sold online due to flammability standards failure, risking burn injuries. Consumers must stop using and return for refund or replacement.
In-ThingsFeb 16, 2022 - Stop using nowConsumer product
Esme Recalls Children's Sleepwear Due to Violation of Federal Flammability Standards and Burn Hazard
Esme recalls four styles of children's sleepwear that fail federal flammability standards, risking burns. Consumers should stop using and return for free replacement or refund.
EsmeFeb 16, 2022 - Stop using nowConsumer product
Anecdote Candles Recalls Double-Wick Autumn Candles Due to Fire and Laceration Hazards; Sold Exclusively at Anthropologie
Anecdote Autumn Glass Candles with double wicks can cause glass breakage, fire, and lacerations. Recalled due to fire and laceration hazards; return to store or follow online instructions for refund.
Anecdote CandlesFeb 16, 2022 - Stop using nowConsumer product
American Landmaster Recalls Utility Vehicles Due to Crash and Injury Hazards
American Landmaster recalls EV, L3, L4, L5, L5W and L7 UTVs made March 2021-Oct 2021 due to steering shaft separation causing loss of control and crash risks. Owners must stop using and contact for inspection or repair.
American LandmasterFeb 16, 2022 - Lower riskMedical device
Wright Medical Technology, Inc. recalls Wright Medical Technology, Inc. ORTHOLOC Non-Locking Screw 2mm x 8mm, REF 5201120008, non-sterile, a component of the
Wright Medical recalls ORTHOLOC Non-Locking Screws (2mm x 8mm) due to incorrect screw packaging. This component is part of the ORTHOLOC 2.0/2.4 Plate System and may contain a locking screw instead of non-locking.
Wright Medical TechnologyFeb 15, 2022 - Use cautionMedical device
Ion Beam Applications S.A. recalls ProteusPLUS and ProteusONE- designed to produce and deliver a proton beam for the treatment of patients with localized
Ion Beam Applications recalls ProteusPLUS and ProteusONE proton therapy systems due to potential risk of incorrect beam range after resuming treatment pauses. This could lead to unintended radiation delivery to patients.
Ion Beam ApplicationsFeb 15, 2022 - Lower riskMedical device
Luminex Corporation recalls VERIGENE Nucleic Acid Test Kit-BC-GN Extraction Tray - 9.73 mL, REF 20-009-021
Luminex recalls specific VERIGENE Nucleic Acid Test Kit extraction trays due to potential no call internal control failures from missing reagents. Affected units include lot 101321021B.
LuminexFeb 15, 2022 - Lower riskMedical device
Meridian Bioscience Inc recalls Revogene, For In Vitro Diagnostic use in performing nucleic acid testing in clinical laboratories. Meridian branded
Meridian Bioscience recalls Revogene lab test kits due to potential false positives in nucleic acid testing. Affected units include all field models with specific catalog numbers.
MeridianFeb 15, 2022 - Use cautionDrug
Macleods Pharma Usa Inc recalls Amlodipine and Olmesartan Medoxomil Tablets, 10 mg /20 mg, 30-count bottles, Rx only, Manufactured for: Macleods Pharma
Macleods Pharma USA recalls specific lots of Amlodipine and Olmesartan Medoxomil tablets due to current Good Manufacturing Practice deviations.
Macleods PharmaFeb 15, 2022 - UnratedDrug
ANI Pharmaceuticals, Inc. recalls Alprazolam Tablets, USP 0.5 mg, packaged in a) 100-count bottles (NDC 67253-901-10), b) 500-count bottles (NDC
ANI Pharmaceuticals recalls 0.5mg Alprazolam tablets with specific NDC codes and expiration dates due to cGMP deviations. Affected products may not meet quality standards.
ANI PharmaceuticalsFeb 15, 2022 - Use cautionMedical device
Biomet, Inc. recalls BIOMET TRAUMA A.L.P.S. FIBULA COMPOSITE LOCKING PLATE 8 HOLE, Item # 856204008. Devices are packaged in a vacuum sealed
Biomet recalls specific fibula plates due to potential packaging failure causing infection risks during surgery. Affected items have item # 856204008 and lot # 913430. Contact for replacement or return.
BiometFeb 14, 2022 - Lower riskMedical device
Cook Medical Incorporated recalls Gunther Tulip Vena Cava Filter Set for Femoral Vein Approach Catalog Number/GPN: IGTCFS-65-1-FEM-TULIP G52917;
Cook Medical is recalling Tulip Vena Cava Filter Sets for Femoral Vein Approach (catalog numbers IGTCFS-65-1-FEM-TULIP, IGTCFS-65-1-JUG-TULIP, IGTCFS-65-1-UNI-TULIP) manufactured from January 24, 2019 through January 24, 2022. This recall includes an update to device descriptions, intended use, contraindications, warnings, precautions, and potential adverse events.
Cook MedicalFeb 14, 2022 - UnratedMedical device
Draeger Medical, Inc. recalls Evita V500 Ventilator with Software 2.51.01 and Lower - intended for the ventilation of adult, pediatric and neonatal
Draeger Medical recalls Evita V500 ventilators with software 2.51.01 and lower due to cybersecurity vulnerabilities. All units are affected; no specific remedy is provided in the recall notice.
DraegerFeb 14, 2022 - Stop using nowMedical device
Baxter Healthcare Corporation recalls Compella Therapy Air Supply Unit
Baxter Healthcare recalls Compella Therapy Air Supply Units due to potential power cord damage causing shock risk. Affected units have specific serial numbers; stop using immediately if you own one.
Baxter HealthcareFeb 14, 2022 - Lower riskMedical device
Cytocell Ltd. recalls Cytocell 8 Square Template Slides (Glass)- microscope slides Reference: PCN008
Cytocell recalls 8 Square Template Slides with incorrect expiry date labels. The correct expiry is February 2022, not May 2023 as shown. Affected items may expire prematurely.
CytocellFeb 14, 2022 - Lower riskDrug
BayCare Integrated Service Center, LLC /dba BayCare Central Pharmacy recalls Norepinephrine bitartrate 16 mg in 250 mL NaCl 0.9%, packaged in IV bags, Rx only, BayCare Central Pharmacy 7802 E.
BayCare Central Pharmacy recalls specific lots of norepinephrine bitartrate 16 mg IV solution (0.9% NaCl) due to subpotent drug. This medication is prescribed only and may not contain enough active ingredient for effective treatment.
BayCare Central PharmacyFeb 14, 2022 - Use cautionVehicle
ENTEGRA ASPIRE (2019) recall — Service Brakes, Air
Entegra is recalling 2015-2019 Aspire motorhomes with undersized air brake reservoirs that may cause reduced braking and crash risk. Owners must have reservoir replaced by dealers.
EntegraFeb 12, 2022 - UnratedFood
Texas Star Nut and Food Co., Inc. recalls Nature's Eats Balance Hearty Mix 16 oz. UPC 832112003842 packaged in cello bag 5 bags per case
Texas Star Nut recalls 16oz Nature's Eats Balance Hearty Mix with undeclared milk. Consumers should check UPC 832112003842 for affected lots. No remedy specified in recall notice.
Texas Star NutFeb 12, 2022 - Use cautionMeat & poultry
Great American Cobbler Company, LLC, Recalls Creole Style Chicken Pot Pie Products Due to Misbranding and an Undeclared Allergen
USDA recalls 4,272 pounds of Creole Style Chicken Pot Pies due to missing soy allergen on labels. Consumers urged to discard products immediately.
Great American CobblerFeb 11, 2022 - Use cautionVehicle
BMW X5 (2023) recall — Visibility
BMW is recalling certain 2023 X5 models due to a potential fire risk from windshield seal short-circuits. Dealers will inspect and repair the seal for free.
BMWFeb 11, 2022 - Use cautionVehicle
VOLKSWAGEN GOLF R (2022) recall — Back Over Prevention
Volkswagen recalls 2022 Golf R models with faulty rearview cameras that may cause crashes due to reduced rear visibility. Owners must contact dealers for free replacement.
VolkswagenFeb 11, 2022 - Use cautionVehicle
VOLKSWAGEN ID.4 (2021) recall — Air Bags
Volkswagen is recalling 2021 ID.4 vehicles with passenger air bags that may not deploy properly in crashes, increasing injury risk. Owners must contact customer service for free replacement.
VolkswagenFeb 11, 2022 - Lower riskMedical device
RaySearch America Inc recalls RayStation 4-11B, and RayPlan 1, 2, 7-11B including some service packs: RayStation 4.0 (4.0.0.14) to RayStation 5
RaySearch America recalls RayStation 4-11B and RayPlan 1-8A software versions due to potential dose errors in radiation treatment planning. Affected users should contact RaySearch for details.
RaySearchFeb 11, 2022 - Use cautionMedical device
Huntleigh Healthcare Ltd. recalls HUNTLEIGH Disposable intraoperative Probe, 8Mhz (box), REF DIPP10, containing 10 individual Disposable Intraoperative
Huntleigh Healthcare recalls disposable intraoperative probes with faceplate detachment risk. Affected units include specific model REF DIPP10, lot 7842006001. Stop using immediately to prevent injury.
Huntleigh HealthcareFeb 11, 2022 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS recalls CombiDiagnost R90 1.1 (709031)
Philips recalls CombiDiagnost R90 1.1 (709031) models where RF viewer may display previous patient radiography images during fluoroscopy, causing image differences. Affected units have specific serial numbers.
PhilipsFeb 11, 2022 - Lower riskMedical device
Abbott Molecular, Inc. recalls Alinity m Integrated Reaction Units (IRU)
Abbott recalls Alinity m Integrated Reaction Units with potential for Reaction Vessels to detach from caps during pipettor robot transport. Affected units have specific lot numbers. Consumers should contact Abbott for details.
AbbottFeb 11, 2022 - Stop using nowDrug
Revive Rx LLC dba Revive Rx Pharmacy recalls HCG 6,000iu (lyo) Human Chorionic Gonadotropin Inj., For Sub-Q or IM Use Only, Not For IV Use, Vial, Rx Only,
Revive Rx recalls HCG 6,000iu injection vials due to bacterial contamination. Check lot numbers and consult your provider immediately.
Revive RxFeb 11, 2022 - Lower riskFood
Malt Products Corporation recalls Diastatic Malt Powder 50lb bag - up to 50 bags per pallet Malt Products Corporation
Malt Products Corporation recalls Diastatic Malt Powder 50lb bags with potential Salmonella contamination. Affected lots include 21L14 and 21L15, expiring June 2022. Consumers should check product details to determine if affected.
Malt Products CorporationFeb 11, 2022
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83,807 recalls tracked · 72,041 explained in plain English · 10,992 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.