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
34,960 found- Use cautionVehicle
CHEVROLET EQUINOX (2019) recall — Seats
Chevrolet is recalling 2019 Equinox vehicles with rear-right seat weld issues that could increase injury risk in crashes. Owners must have seatback frame replaced free by dealers.
ChevroletJul 3, 2019 - Lower riskMedical device
Heidelberg Engineering GmbH recalls SPECTRALIS with HEYEX2 image management system. a non-contact ophthalmic diagnostic imaging device.
Heidelberg Engineering recalls SPECT: A non-contact ophthalmic diagnostic device with HEYEX2 image management system that may display incorrect patient data due to a software configuration error.
Heidelberg EngineeringJul 3, 2019 - Use cautionMedical device
Elekta Inc recalls Monaco RTP System, software versions 5.10 and 5.11, Radiation Treatment Planning System
Elekta recalls Monaco RTP software versions 5.10 and 5.11 due to potential incorrect monitor unit scaling during radiation treatment planning. Affected units may require software update to prevent treatment errors.
ElektaJul 3, 2019 - Lower riskMedical device
LivaNova USA Inc. recalls LivaNova SMART PERFUSION PACK INSPIRE 8S - Product Usage: The affected product is a perfusion tubing pack use in
LivaNova recalls SMART PERFUSION PACK INSPIRE 8S tubing packs with incorrect cuvette packaging. Affected units have model 046008200 and lot 19121:100141. No remedy specified in recall notice.
LivaNovaJul 3, 2019 - Lower riskMedical device
PediaLift LLC recalls PediaLift Access Device, Device Identifier: B751PDLFT0
PediaLift recalls 12 units of Access Device (serial numbers PCL-HDPE-DL-1 to PCL-HDPE-DL-12) due to missing compliance certificate. No action needed as the hazard is non-operational.
PediaLiftJul 3, 2019 - Lower riskMedical device
Capso Vision, Inc. recalls CapsoCam Plus *** System, Imaging, Gastrointestinal, Wireless, Capsule, Electrical Rating 3.1V DC/10mA REF 2795 -
Capso recalls specific models of wireless gastrointestinal capsule systems due to possible mislabeling with incorrect serial numbers, which could lead to patient misdiagnosis. Affected units have unique serial numbers starting with A00ZD4.699.
CapsoJul 3, 2019 - Lower riskMedical device
Xcision Medical Systems, LLC recalls GammaPod Stereotactic Radiotherapy System Model A, REF XMSGP030A00-0.02 Product Usage: GammaPod is a teletherapy device
Xcision Medical Systems recalls GammaPod Stereotactic Radiotherapy System Model A (serials GP0002, GP0004) due to alignment drift causing reduced radiation dose output. Affected users should contact for remedy.
Xcision Medical SystemsJul 3, 2019 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls SOMATOM Definition AS, Model Number 8098027 - Product Usage: Computed tomography systems intended to generate and
Siemens recalls specific model CT scanners that may cause scan abortions due to software issues with syngo.CT version VB10A. Affected units include serial numbers listed in the recall notice.
SiemensJul 3, 2019 - Stop using nowMedical device
Valeritas, Incorporated recalls DEMO No Needle Corrugated Carton 20 U/D, Part Number 2260-03
Valeritas recalls 20-unit demo cartons with potential needle contamination. Affected units have specific lot numbers and part numbers. Stop using immediately to avoid injury.
Valer:itasJul 3, 2019 - Use cautionFood
Topway Enterprises, Inc recalls Salmon (Cut)
Topway Enterprises recalls salmon cuts potentially contaminated with Listeria monocytogenes. Consumers should avoid eating these products to prevent foodborne illness.
TopwayJul 3, 2019 - Use cautionConsumer product
The Company Store Recalls Girl's Pajama Sets Due to Violation of Federal Flammability Standard (Recall Alert)
The Company Store recalls girl's pajama sets that fail federal flammability standards, risking burn injuries. Consumers should stop using and get a refund.
The Company StoreJul 3, 2019 - Use cautionConsumer product
Nature's Truth Recalls Wintergreen Essential Oil Due to Failure to Meet Child Resistant Closure Requirements
Nature's Truth recalls wintergreen essential oil bottles that aren't child-resistant, posing poisoning risk to young children. Consumers should remove from reach and get refunds.
Nature's TruthJul 3, 2019 - Stop using nowConsumer product
Just Love Fashion Recalls Children's Pajama Pants Due to Violation of Federal Flammability Standard (Recall Alert)
Just Love Fashion recalls Prince of Sleep children's fleece pajama pants due to flammability risks. Check labels and get a refund.
Prince of SleepJul 3, 2019 - Use cautionVehicle
KTM 1290 SUPER ADVENTURE (2016) recall — Fuel System, Gasoline
KTM recalls 2015-2016 1290 Super Adventure motorcycles with potential fuel leaks near ignition sources, risking fire. Owners must have fuel tank cover mounting insert inspected and replaced free by dealers.
KTMJul 2, 2019 - Use cautionVehicle
CHEVROLET SILVERADO 3500 (2018) recall — Fuel System, Gasoline
General Motors recalls 2018 Chevrolet Silverado 3500 trucks with fuel system issues that could cause tank overfill, leading to potential fire risks. Owners must have the front tank inspected or replaced at no cost.
ChevroletJul 2, 2019 - Use cautionVehicle
CADILLAC CTS (2018) recall — Steering
General Motors recalls 2018 Cadillac CTS vehicles with potential power steering failure, increasing crash risk at low speeds. Owners must have power steering gear assembly replaced free by dealers.
CadillacJul 2, 2019 - Use cautionVehicle
FREIGHTLINER CASCADIA (2020) recall — Air Bags
Daimler Trucks is recalling 2018-2020 Freightliner Cascadia trucks with optional steering wheel air bags that may deploy unexpectedly, increasing crash risk. Owners should contact DTNA for free air bag removal.
Daimler TrucksJul 2, 2019 - UnratedMedical device
Mazor Robotics Ltd recalls Snapshot Tracker Kit, Mas2659-01, KIT0898, Rx Only, Non Sterile, UDI: 07290109181868
Mazor Robotics recalls Snapshot Tracker Kit (Lot Numbers 070494-070548) due to potential navigational inaccuracies that could cause patient injury like nerve damage. Affected users should contact for remedy.
Mazor RoboticsJul 2, 2019 - Lower riskMedical device
Roche Diagnostics Operations, Inc. recalls The Tina-Quant Myoglobin Gen. 2 Tests system is an immuno-turbidimetric assay for the quantitative in vitro
Roche recalls Tina-Quant Myoglobin Gen 2 Tests (lot 349860+) due to calibration failures and QC imprecision from signal drop in reaction kinetics. Affected units may produce inaccurate results.
RocheJul 2, 2019 - Use cautionMedical device
GE Healthcare, LLC recalls Refurbish RIC5-9-D Probe ROHS compliant Ultrasound Probe RIC5-9-D
GE Healthcare recalls specific Refurbish RIC5-9-D ultrasound probes due to potential transvaginal transducer misalignment. Affected models include KTZ303987-R with serial numbers starting with 226914KR0, 198026KR7, 220616KR7, and 205375KR9. Contact GE Healthcare for details.
GE HealthcareJul 2, 2019 - Lower riskMedical device
Qiagen Sciences LLC recalls QIAsymphony SP SOW 5.0.3, software used with the QIAsymphony SP Instrument (The QIAsymphony SP instrument is designed
Qiagen recalls software version 5.0.3 for QIAsymphony SP instruments due to potential incorrect patient reporting if 2D bar codes aren't verified before downstream applications. Affected units include specific serial numbers listed in the recall.
QiagenJul 2, 2019 - Lower riskMedical device
Cincinnati Sub-Zero Products LLC, a Gentherm Company recalls CoolBlue Hyper-Hypothermia System- body hypothermia system Model: Innercool - Product Usage: The system is composed of
Cincinnati Sub-Zero recalls CoolBlue Hyper-Hypothermia System Model Innercool due to risk of tissue damage from overheating beyond 40°C. Affected units have serial numbers 073-CB-00001 to 162-CB-00294.
Cincinnati Sub-ZeroJul 2, 2019 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151812
Zimmer Biomet recalls Orthopedic Salvage System Hybrid Poly Tibia Item #151812 due to potential ineffective cleaning processes. Affected products were distributed from June 2016 to February 2019.
Zimmer BiometJul 2, 2019 - UnratedDrug
Lupin Pharmaceuticals Inc. recalls Kaitlib Fe norethindrone and ethinyl estradiol chewable tablets (0.8 mg/0.025 mg) and Ferrous Fumarate, Chewable
Lupin Pharmaceuticals recalls Kaitlib Fe norethindrone and ethinyl estradiol chewable tablets due to impurities found in stability testing. This may cause serious health risks. Consumers should contact the company for details.
Lupin PharmaceuticalsJul 2, 2019 - UnratedDrug
Altaire Pharmaceuticals, Inc. recalls CVS Health Redness Relief Lubricant Redness Reliever Eye Drops, Sterile, 1 fl. oz., (30 mL), Distributed by: CVS
Altaire Pharmaceuticals recalls CVS Health Redness Relief Lubricant Eye Drops due to potential lack of sterility. Consumers should check lot numbers on packaging for affected batches.
Altaire PharmaceuticalsJul 2, 2019 - Stop using nowConsumer product
SRAM Recalls RockShox Front Suspension Forks Due to Crash and Injury Hazards
SRAM recalls RockShox Lyrik and Yari front suspension forks with serial numbers 02T95514009 to 08T96214665 due to risk of breakage causing loss of control and crashes. Consumers must stop using and get free replacements.
SRAMJul 2, 2019 - Stop using nowConsumer product
Electric Bicycles Recalled by Faraday; Seat Post Poses Fall Hazard
Faraday recalls Porteur, Cortland e-bikes due to seat posts that can break. Stop using immediately and contact Faraday for a free replacement.
FaradayJul 2, 2019 - Use cautionVehicle
MCI J4500 (2012) recall — Steering
MCI recalls 2012 J4500 coaches with hydraulic steering systems that may lock, causing loss of steering control. Owners must contact MCI for free axle alignment repairs.
MCIJul 1, 2019 - Stop using nowVehicle
TESLA MODEL S (2014) recall — Air Bags
Tesla is recalling 2014-2016 Model S vehicles with certain passenger air bag inflators that may explode during deployment, causing serious injury or death. Owners must have air bags replaced free of charge by Tesla Service Centers.
TeslaJul 1, 2019 - Stop using nowVehicle
FORD MUSTANG (2014) recall — Air Bags
Ford is recalling 2014 Mustang vehicles with potential passenger air bag inflator explosions causing serious injury or death. Owners must stop driving until repair is done.
FordJul 1, 2019
Browse recalls
- Recalls by vehicle make & model
- Pet food recalls
- Drug shortages
- September 2026 recall report
- All monthly reports
83,517 recalls tracked · 71,995 explained in plain English · 10,969 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.