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
34,894 found- Lower riskMedical device
LivaNova USA recalls Inspire 8 Integrated Phisio OXY w/ HVR Reservoir, Sterile EO, Catalog # 050714 The intended uses for the two elements
LivaNova recalls Inspire 8 Integrated Phisio OXY with HVR Reservoir due to incorrect expiration date printed in the UDI barcode. The expiration date is listed as DDMMYY instead of YYMMDD, though package labels show correct dates.
LivaNovaMar 13, 2018 - Use cautionMedical device
Keystone Dental Inc recalls Genesis Surgical Cassette Tapered Implants are intended for placement following natural tooth loss or for immediate
Keystone Dental recalls Genesis Surgical Cassette Tapered Implants with extra-large white grommets that may cause dental burs to wobble, potentially leading to injury during dental procedures.
Keystone DentalMar 13, 2018 - Lower riskMedical device
Medtronic Vascular recalls Medtronic DxTerity Diagnostic Catheter, JL 4.0, REF DXT5JL40, marked with 6F color code on box.
Medtronic recalls specific DxTerity Diagnostic Catheters due to potential incorrect size labeling on the box, which could lead to improper use. Affected units have a 6F color code on the box but are labeled 5F inside.
Medtronic VascularMar 13, 2018 - Lower riskFood
Mondelez Global Llc recalls Sour Patch Kids, 1.9 lb bag
Mondelez recalls Sour Patch Kids 1.9 lb bags after finding peanut shells in a small batch during repacking. The product is not labeled as containing peanuts but may pose a risk for peanut allergies.
MondelezMar 13, 2018 - Lower riskFood
Premier Food Management, LLC recalls Chicken bacon, egg white and cheese on flat bread sandwich
Premier Food Management recalls chicken bacon, egg white and cheese on flat bread sandwiches made with raw chicken bacon. Consumers should avoid these products due to potential food safety risks.
Premier Food ManagementMar 13, 2018 - Stop using nowConsumer product
MAAX Spas Recalls Hot Tubs and Swim Spas Due to Fire Hazard
MAAX Spas recalls hot tubs and swim spas with Delta UV generator model EA-4H-5 due to fire risk. Consumers must stop using and contact a dealer for free repair.
MAAX SpasMar 13, 2018 - Use cautionConsumer product
Helvetia Sports Recalls SwissStop Bicycle Disc Brake Pads Due to Fall Hazard
SwissStop recalls EXOTherm cycling disc brake pads that can separate from backplate, causing fall hazards. Return to store for full refund.
SwissStopMar 13, 2018 - Stop using nowConsumer product
Amazon Recalls Portable Power Banks Due to Fire and Chemical Burn Hazards (Recall Alert)
Amazon recalls six models of portable power banks due to fire and chemical burn risks. Affected units may overheat and ignite, causing injury. Consumers should stop using and return for refund.
AmazonBasicsMar 13, 2018 - Use cautionVehicle
FOREST RIVER SALEM (2019) recall — Exterior Lighting
Forest River is recalling 2019 Salem trailers with faulty clearance lights that may not work due to incorrect wiring, increasing crash risk. Owners should contact customer service for free repairs.
Forest RiverMar 12, 2018 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Syva¿ EMIT¿ II Plus 6-Acetyl morphine Catalog # for 28 mL: 9R039UL /SMN# 10470440
Siemens Healthcare recalls Syva EMIT II Plus 6-Acetyl morphine 28mL catalog #9R039UL for incorrect calibrator level in calibration steps. No remedy specified in recall notice.
Siemens HealthcareMar 12, 2018 - Lower riskMedical device
Ohio Medical Corporation recalls Vacuum Regulator, Push-T-Set Intermittent Suction Unit (PTS-ISU) Product Usage: The vacuum regulator is intended to be
Ohio Medical Corporation recalls vacuum regulators for incomplete quality control testing. Affected units have specific model numbers and lot numbers. Consumers should contact the company for details.
Ohio Medical CorporationMar 12, 2018 - Lower riskMedical device
TMJ Solutions Inc recalls Patient-Fitted Temporomandibular (TMJ) Right Mandibular Component part of TMJ Reconstruction Prosthesis System. Model
TMJ Solutions recalls a specific TMJ reconstruction prosthesis component due to mislabeling. This incorrect part may not fit the patient's needs, risking improper use. Affected units include model TYY-NNNNRM with lot W43963 and serial T170939RM.
TMJ SolutionsMar 12, 2018 - Lower riskMedical device
CooperSurgical, Inc. recalls 5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar - extended length (5 count); Model Number 900-840 Product Usage:
CooperSurgical recalls 5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar (Model 90: 223333) due to incorrect packaging. This may cause improper surgical use. Affected users should contact CooperSurgical for details.
CooperSurgicalMar 12, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Phoenix Nail System, intended for use with an intramedullary nail system for alignment, stabilization and fixation of
Zimmer Biomet recalls certain Phoenix Tibia Nail 3.5mm Inserter instruments manufactured before March 30, 2017 due to reports of fracturing and remaining in the device implant after surgery.
Zimmer BiometMar 12, 2018 - Stop using nowMedical device
Stryker Medical Division of Stryker Corporation recalls Power-LOAD Cot Fastening System, Model #6390, Catalog #6390-000-000, UDI: 07613327261523 Power-LOAD is intended to
Stryker recalls Power-LOAD Cot Fastening System Model #6390 due to risk of broken floor plates during ambulance transport. Affected units have specific serial numbers. Stop using immediately to prevent potential injury.
StrykerMar 12, 2018 - Lower riskMedical device
CooperSurgical, Inc. recalls Fischer Cone Biopsy Excisor, Medium (5/Box); Model Number: 900-151
CooperSurgical recalls Fischer Cone Biopsy Excisor Medium (5/Box) model 900-151 due to incorrect packaging. Consumers should check product details to determine if affected.
CooperSurgicalMar 12, 2018 - Lower riskMedical device
McKesson Israel Ltd. recalls McKesson Cardiology Hemo, Release SW version 13.0. Used for physiological monitoring, image and data processing.
McKesson Cardiology Hemo software version 13.0 may not display physiological signals under certain conditions. Affected units were sold for clinical monitoring and data processing. Contact McKesson for remedy.
McKesson Cardiology HemoMar 12, 2018 - UnratedMedical device
Stryker GmbH recalls Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation of fractures, joint contractures, fusions, limb
Stryker recalls Hinge Coupling Hoffmann LRF Catalog #4933-0-800 due to wrong parts being packed in packaging. This affects pediatric and adult patients needing fracture fixation. No remedy specified in official notice.
StrykerMar 12, 2018 - Use cautionMedical device
Hamilton Medical AG recalls Hamilton-C2 Ventilator Unit Intended to provide ventilator support to adults and pediatrics and optionally infants and
Hamilton Medical recalls C2 Ventilators due to battery gauge potentially showing higher charge than actual. This could lead to unexpected shutdowns during critical care. Affected units have serial numbers and were sold in hospitals.
Hamilton MedicalMar 12, 2018 - Stop using nowMedical device
Micro-Tech (Nanjing) Co., Ltd. recalls Trident Endoscopic Ultrasonic Biopsy Needle (FNB)
Micro-Tech recalls Trident Endoscopic Ultrasonic Biopsy Needles (FNB) due to potential breakage in the body causing injury. Affected units have specific identifiers; stop using if you own one.
Micro-TechMar 12, 2018 - Stop using nowFood
Food and Beverage Inc. recalls Name: Trader Joe s Chocolate Chip Cookies SKU 68075 Net Weight: 12 oz. (340g) Number of units per package: 16 cookies
Trader Joe's is recalling 12 oz bags of Chocolate Chip Cookies (SKU 68075) because they contain peanut butter, posing a serious risk to those with peanut allergies.
Trader Joe'sMar 12, 2018 - Lower riskMedical device
Richard Wolf GmbH recalls RICHARD WOLF TUBE SET FOR TEM, REF 4170.801. Used for the transanal endoscopic microsurgery.
Richard Wolf recalls tube set model 4170.801 for transanal endoscopic surgery due to risk of mixed tube ends. Affected units have specific lot numbers.
Richard WolfMar 11, 2018 - Lower riskFood
Schwartz Brothers Restaurants dba Schwartz Brothers Bakery recalls Gourmet Cream Cheese Cinnamon Rolls, packaged in a 16 oz. plastic clam shell container and sold under the Schwartz
Schwartz Brothers Bakery recalls Gourmet Cream: Undeclared egg in cinnamon rolls may cause allergic reactions. Stop using if you have egg allergies.
SchwartzMar 11, 2018 - Use cautionVehicle
SPARTAN METROSTAR (2017) recall — Equipment
Spartan is recalling 2017 MetroStar emergency vehicles with improperly sized mounting fasteners that could allow EMS cabinets to become projectiles during crashes.
SpartanMar 10, 2018 - Use cautionFood
Lancaster Fine Foods Inc. recalls 1.5 oz. cup with seal on label reading: Thai Sweet Chili Sauce; Ingredients: Thai Sweet Chili Sauce (Sugar, Water,
Lancaster Fine Foods recalls 1.5 oz cups of Thai Sweet Chili Sauce because they were mislabeled as Spicy Mayonnaise Sauce, posing an allergy risk.
Lancaster Fine FoodsMar 10, 2018 - Lower riskFood
Wegmans Food Markets, Inc. recalls Wegmans Assorted Gyoza (Dumplings), Family Pack, 17 oz. UPC: 2-48798-00000 or 2-48963-00000 packaged with Wegmans Thai
Wegmans recalls family packs of gyoza with Thai sauce that contain undeclared egg. Consumers should check UPCs 2-48798-00000 or 2-48963-00000 and avoid eating if allergic.
WegmansMar 10, 2018 - Lower riskFood
Maplehurst Bakeries, LLC. recalls ITALIAN BREAD, SKU: 10424, Frozen Dough
Maplehurst Bakeries recalls Italian Bread (SKU 10424) due to potential Listeria monocytogenes contamination from raw wheat gluten. Consumers should check best before date and contact for details.
Maplehurst BakeriesMar 10, 2018 - Use cautionMeat & poultry
Heartland Catfish Company Recalls Siluriformes Fish Products Due to Possible Adulteration
USDA FSIS recalls 69,016 pounds of Heartland Catfish products for possible leucomalachite green residue. Consumers urged not to consume or dispose of recalled items.
Heartland Catfish CompanyMar 9, 2018 - Lower riskMedical device
St. Jude Medical, Inc. recalls Proclaim DRG Implantable Pulse Generator, Model Number 3664
St. Jude Medical recalls Proclaim DRG Implantable Pulse Generator model 3664 due to error messages during impedance checks and transient overstimulation causing patient discomfort. Affected units have specific lot and serial numbers.
St. Jude MedicalMar 9, 2018 - Use cautionMedical device
Hamilton Medical AG recalls Hamilton-C3 Ventilator Unit Product Usage: The HAMILTON-C3 ventilator is intended to provide positive pressure
Hamilton Medical recalls C3 ventilators with potential for unintended shutdown due to control board issues. Affected units may shut down unexpectedly with alarms. Contact for remedy details.
Hamilton MedicalMar 9, 2018
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83,390 recalls tracked · 71,917 explained in plain English · 10,946 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.