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
SEAFARERS INC recalls Frozen Yellowfin Tuna Loins, Vacuum Packed, Imported and Distributed by Seafarers, Inc, 5-8 LBS, Product of Vietnam
Seafarers Inc recalls frozen yellowfin tuna loins (5-8 lbs) from Vietnam due to four reported illnesses with rash, stomach cramps, and diarrhea. Consumers should check lot numbers.
SeafarersSep 17, 2020 - Lower riskFood
Homestead Creamery, Inc. recalls All Natural Chocolate Pecan ice cream, 2.5 gallons, UPC:7525200120. Packaged in a plastic container
Homestead Creamery recalls 2.5-gallon All Natural Chocolate Pecan ice cream with undeclared pecans. Consumers should check UPC 7525200120 for affected products.
Homestead CreamerySep 17, 2020 - Use cautionMeat & poultry
Willow Tree Poultry Farm, Inc. Recalls Ready-To-Eat Chicken Salad Products due to Misbranding and an Undeclared Allergen
USDA recalls 6,890 pounds of ready-to-eat chicken salad products for misbranding and undeclared walnuts allergen. Consumers urged not to consume or discard items.
Willow Tree Poultry FarmSep 16, 2020 - Use cautionVehicle
VOLKSWAGEN GOLF R (2018) recall — Unknown Or Other
Volkswagen recalls 2018 Golf R vehicles that may not meet safety standards, increasing crash risk. Owners must contact customer service for repurchase.
VolkswagenSep 16, 2020 - Use cautionVehicle
KIA STINGER (2020) recall — Fuel System, Gasoline
Kia recalls certain 2020-2021 Stinger vehicles due to a potential fuel pump issue that could cause engine power loss and increase crash risk. Owners should contact Kia for free repairs.
KiaSep 16, 2020 - Use cautionMedical device
Boston Scientific Corporation recalls Hurricane RX Biliary Balloon Dilatation Catheter Catalog REF No. M00545890; M00545900; M00545910; M00545920; M00545930;
Boston Scientific recalls Hurricane RX Biliary Balloon Dilatation Catheters with specific model numbers and batch dates due to risk of the black sheath detaching from the catheter shaft.
Boston ScientificSep 16, 2020 - Use cautionMedical device
Merit Medical Systems, Inc. recalls MeritMedical Cultura Flex Swab, Sterile Flocked Collection Device, Ref C100F, Sterile, for the following unit count:1
Merit Medical recalls Cultura Flex Swab (Ref C100F) due to flocked tip breaking off during use, potentially causing soft tissue injury or treatment delays. Affected units sold before August 28, 2020.
Merit MedicalSep 16, 2020 - Lower riskDrug
Arbor Pharmaceuticals Inc. recalls Nymalize (nimodipine) oral solution, 60 mg/20 mL, 12 Unit-Dose Cups and 12 Oral Syringes, 2 inner cartons per outer
Arbor Pharmaceuticals recalls Nymalize oral solution (60 mg/20 mL) due to subpotent drug levels. This may not provide intended treatment. Contact for return instructions.
Arbor PharmaceuticalsSep 16, 2020 - Lower riskDrug
Perrigo Company PLC recalls Albuterol Sulfate Inhalation Aerosol, 90 mcg per actuation, 200 metered inhalations, Manufactured by: Catalent Pharma
Perrigo recalls Albuterol Sulfate Inhalers with defective delivery systems that may fail to dispense medication consistently. Affected units have specific NDC codes and expiration dates listed in the recall notice.
PerrigoSep 16, 2020 - Lower riskDrug
Calvin Scott & Company, Inc. recalls Diethylpropion, 25 mg tablets, Rx only, Distributed by: Calvin Scott & Co. Inc. Albuquerque, NM 87123; MFG. Lannett
Calvin Scott recalls 25mg Diethylpropion tablets (Rx only) repackaged without stability testing. Affected lots expire by Dec 2020 or later. Consumers should contact manufacturer for details.
Calvin ScottSep 16, 2020 - Stop using nowConsumer product
RH Recalls Industrial Three-Panel Mirrors Due to Injury Hazard
RH recalls industrial three-panel mirrors due to panels detaching and falling, causing injury. Affected models sold with specific SKUs; stop using and get refund or credit.
RHSep 16, 2020 - Stop using nowConsumer product
MWE Investments Recalls Westinghouse Portable Generators Due to Fire Hazard
Westinghouse recalls two models of dual fuel portable generators (2019) due to fuel leaks causing fire and burn risks. Consumers must stop using and contact MWE Investments for free repairs.
WestinghouseSep 16, 2020 - Stop using nowConsumer product
Monoprice Recalls Ethernet Cables Due to Fire Hazard
Monoprice recalls Category 6 Ethernet Bulk CMR cables due to fire risk when exposed to flame. Consumers must stop using and replace these cables at no cost.
MonopriceSep 16, 2020 - Use cautionVehicle
THOR MOTOR COACH ARIA (2020) recall — Tires
Thor Motor Coach is recalling certain 2018-2021 Aria motorhomes for potential tire valve stem damage that could cause loss of tire pressure and increase crash risk. Owners should contact TMC or DTNA for free inspections or replacements.
Thor Motor CoachSep 15, 2020 - Lower riskMedical device
3M Company - Health Care Business recalls 3M Red Dot Monitoring Electrode with Foam Tape - Product Usage: intended to be used by healthcare professionals for ECG
3M recalls 1000 ECG electrodes with foam tape due to corrosion risk causing performance failures. Healthcare professionals should check product lot numbers and contact 3M for details.
3MSep 15, 2020 - Lower riskMedical device
Medline Industries Inc recalls Quick Release Gait Belt, 60
Medline recalls Quick Release Gait: Gait belts with model MDT821208NATM/503689 may have buckles that break due to gamma radiation exposure. Affected lots include 33019040001, 33019090001, and 33019100001.
MedlineSep 15, 2020 - Lower riskMedical device
Percussionaire Corporation recalls Monitron II Waveform Analyzer, REF: S00015-1, used with ventilators.
Percussionaire recalls Monitron II Waveform Analyzers (REF S00015-1) used with ventilators due to screen freezes that may cause display issues during critical medical monitoring.
PercussionaireSep 14, 2020 - Lower riskMedical device
Philips North America, LLC recalls Philips Sterilizable Defibrillator Paddles, Switched Internal Paddles, Model Numbers M4741A, M4742A, M4743A, M4744A -
Philips recalls sterilizable defibrillator paddles (models M4741A-M4744A) produced 2015-2020 due to potential failure in paddle checks during use. The addendum provides a specific test to detect this issue.
PhilipsSep 14, 2020 - Lower riskMedical device
Becton Dickinson & Company recalls Bard 3F SL PowerMidline Full Kit CE-indicated for short term access to the peripheral venous system for selected
Becton Dickinson recalls Bard 3F SL PowerMidline Full Kits due to missing stylet/T-lock assembly, which could lead to procedural delays or kit discards during IV procedures.
Becton DickinsonSep 14, 2020 - Lower riskMedical device
Medline Industries Inc recalls Kit Model #650301018, MTO Vascular Surgery - Cleveland Clinic PG - Product Usage: NAMIC Cath Lab and Interventional
Medline recalls specific vascular surgery kits that were sold to facilities without sterilization capabilities, posing a risk of infection due to non-sterile use.
MedlineSep 14, 2020 - Lower riskMedical device
Invivo Corporation recalls MR Coils The MR Coil is intended to be used in conjunction with a Magnetic Resonance Scanner to produce diagnostic
Invivo Corporation recalls MR Coils with mistakenly printed IPX1 water rating labels. These coils are used with MRI scanners. Affected models include dS Knee Sch 1.5T, dS Shoulder Sch 3.0T, and others. No action is required as the labels are incorrect but not dangerous.
InvivoSep 14, 2020 - Use cautionMedical device
Becton Dickinson & Company recalls BD Nexiva Closed IV Catheter System Dual Port (20 GA 1.75 IN) Catalog (Ref) No. 383538 BD Nexiva closed IV catheter
Becton Dickinson recalls BD Nexiva Closed IV Catheter Systems with dull needles that could delay treatment. Learn if your product is affected and what to do.
Becton DickinsonSep 14, 2020 - Use cautionVehicle
AUDI RS5 (2019) recall — Electrical System
Audi is recalling certain 2018-2019 RS5 coupes due to a faulty battery cover that may prevent doors from opening after a rear crash, increasing injury risk.
AudiSep 12, 2020 - Use cautionVehicle
BMW X5 (2021) recall — Electrical System
BMW is recalling certain 2021 X5 models due to potential fire risk from improper electrical connections. Affected vehicles may need a free battery and starter-generator repair by dealers starting April 12, 2021.
BMWSep 12, 2020 - Use cautionMedical device
Fresenius Medical Care Holdings, Inc. recalls Liberty Select Cycler Software Version 2.9.0 Model Number 180343 and RTLR180343
Fresenius recalls Liberty Select Cycler software version 2.9.0 (model 180343/RTLR180343) due to potential dialysis solution shortage causing toxin buildup. Affected users should contact for remedy.
Fresenius Medical CareSep 12, 2020 - Lower riskMeat & poultry
Cher-Make Sausage Company Recalls Fully Cooked Meat Sausage Products Due to Misbranding and an Undeclared Allergen
USDA recalls Cher-Make Sausage products due to undeclared cheese in fully cooked sausages. Consumers urged not to eat recalled items.
Cher-Make SausageSep 11, 2020 - Use cautionVehicle
THOMAS BUILT BUSES MINOTOUR (2018) recall — Equipment Adaptive/Mobility
Daimler Trucks North America recalls 2008-2021 Thomas Built Buses Minotour school buses due to wheelchair lift deployment risk during gear shifts. Owners must contact DTNA for free wiring modifications to prevent injury.
Thomas Built BusesSep 11, 2020 - Lower riskMedical device
Fujifilm Medical Systems U.S.A., Inc. recalls Synapse PACS Software Versions 5.1 and higher
Fujifilm recalls Synapse PACS software versions 5.1 and higher due to risk of displaying incorrect patient information or SUV values in medical imaging. Affected users should contact the manufacturer for updates.
Fujifilm Medical SystemsSep 11, 2020 - Lower riskMedical device
Fujifilm Medical Systems U.S.A., Inc. recalls Synapse PACS Software Version 5.6.1 - Product Usage: intended for use as a web based application on an off-the shelf PC
Fujifilm recalls Synapse PACS Software Version 5.6.1 due to potential over-reporting of 3D Sphere MAX values in CT studies. Affected users should contact Fujifilm for guidance.
FujifilmSep 11, 2020 - Lower riskMedical device
RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) recalls Streamline MIS Navigation System Taps, Catalog numbers 04-CANNDRILL-MDN 04-CANNTAP-40-MDN 04-CANNTAP-45-MDN
Pioneer Surgical Technology recalls Streamline MIS Navigation System Taps (catalog numbers 04-CANNDRILL-MDN, 04-CANNTAP-40-MDN, etc.) due to incompatibility with Streamline MIS tap sleeves. Affected units may cause improper function during surgery.
Pioneer Surgical TechnologySep 11, 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.