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
35,025 found- Use cautionVehicle
POLESTAR POLESTAR 2 (2021) recall — Electrical System
Polestar is recalling certain 2021-2022 Polestar 2 vehicles due to a potential high voltage system disconnect that could cause loss of drive power and increase crash risk. Owners will receive free software updates via dealer or over-the-air.
PolestarFeb 24, 2021 - Use cautionVehicle
INTERNATIONAL LT (2021) recall — Engine
Navistar recalls 2021 International LT trucks with Cummins X15 engines due to potential flywheel detachment causing crash risk. Owners must contact Navistar for free repairs.
NavistarFeb 24, 2021 - Use cautionVehicle
AUDI A8 (2020) recall — Engine And Engine Cooling
Audi is recalling 2019-2021 A8 and 2020-2021 S8 vehicles due to a missing sealing pin in the engine control module connector that may cause engine stalling and crash risk. Free repairs available.
AudiFeb 24, 2021 - Use cautionMedical device
Philips Healthcare (Suzhou) Co., Ltd. recalls Philips CT systems are advanced continuous-rotation computed tomography systems suitable for a wide range of computed
Philips Healthcare recalls CT systems with Incisive CT couch that may fail to self-lock, causing unexpected downward movement. Affected units have specific Unique Device Identifiers.
Philips HealthcareFeb 24, 2021 - Lower riskMedical device
Arthrex, Inc. recalls Drill Bit, Cannulated, 5.0 mm - Product Usage: may be used in a variety of foot and ankle procedures.
Arthrex recalls 5.0mm cannulated drill bits with incorrect color indicators for foot and ankle procedures. Affected units have product code AR-8770-02 and lot number 032052.
ArthrexFeb 24, 2021 - Lower riskMedical device
Microbiologics Inc recalls KWIK-STIK, Candida parapsilosis derived from ATCC 22019, REF 0726P. Packaged 2 units per pack. IVD controls.
Microbiologics recalls KWIK-STIK IVD controls with potential labeling error in lot 726-57-10. Affected units may have incorrect packaging labels.
MicrobiologicsFeb 24, 2021 - Lower riskMedical device
Access Vascular, Inc. recalls Scalpel and StatLock included with HydroPICC Catheter Kit - PICC-142, Peripherally Inserted Central Catheter
Access Vascular recalls HydroPICC Catheter Kit (PICC-142) with Scalpels and StatLocks that have shorter expiration dates than listed on the outer package. Consumers should check kit lot numbers and expiration dates.
Access VascularFeb 24, 2021 - Lower riskMedical device
Microbiologics Inc recalls KWIK-STIK, Enterobacter cloacae subsp. cloacae derived from ATCC 13047, REF 0323P. Packaged 2 units per pack. IVD
Microbiologics recalls KWIK-STIK IVD controls with lot 323-108-7 due to incorrect labeling. Affected units may have wrong product code, but no safety risk is reported. Check your lot number for recall.
MicrobiologicsFeb 24, 2021 - Lower riskFood
Mediterranean Food, Inc. recalls Alqosh Sesame Oil "Tahin" packaged in 2lb plastic jars
Mediterranean Food Inc. recalls 2lb sesame oil jars due to Salmonella contamination. Consumers should avoid using affected products.
Mediterranean FoodFeb 24, 2021 - Stop using nowConsumer product
Urban Outfitters Recalls Margo Taper Candle Holders Due to Fire Hazard
Urban Outfitters recalls Margo Taper Candle Holders due to fire risk from candle flame contact. Affected units include small, medium, and large sizes with specific SKU numbers. Return for full refund or prepaid label.
Urban OutfittersFeb 24, 2021 - Stop using nowConsumer product
SmartPool Recalls Children's Multi-Purpose Helmets Due to Risk of Head Injury
Bee Free children's helmets sold in small sizes (head circumference 48-53 cm) pose head injury risk for children aged 2-4. Consumers should stop using and get a refund.
Bee FreeFeb 24, 2021 - Use cautionConsumer product
Potter Electric Recalls Addressable Pull Stations Single/Dual Action Due to Failure to Alert to Fire
Potter Electric recalls addressable pull stations that may fail to activate fire alarms when pulled, risking undetected fires. Affected models include single and dual action units with specific date codes.
Potter ElectricFeb 24, 2021 - Stop using nowConsumer product
Northern Tool & Equipment Recalls Powerhorse Portable Generators Due to Shock Hazard
Northern Tool recalls Powerhorse 13000ES portable generators due to electrical shock risk. Consumers must stop using and get free repairs.
Northern ToolFeb 24, 2021 - Lower riskMedical device
Trinity Sterile, Inc. recalls Midline Catheter Dressing Change Kit with Statlock - Product Usage: Intended to provide ongoing vascular catheter
Trinity Sterile recalls Midline Catheter Dressing Change Kits with Statlock due to face masks or materials in the seal, risking infection. Affected kits have Product Number TRIO0000l and Lot Number 60:0001.
Trinity SterileFeb 23, 2021 - Use cautionMeat & poultry
GLG Trading Inc., Recalls Beef Tallow Products Imported Without the Benefit of Inspection
USDA FSIS recalls 96,810 lbs of beef tallow hotpot seasonings imported from China without inspection. Consumers urged not to consume or dispose of products.
Ming YangFeb 22, 2021 - Use cautionVehicle
MAZDA MAZDA3 (2021) recall — Tires
Mazda recalls 2021 Mazda3 vehicles with potential sudden tire air valve leaks that could cause loss of vehicle control. Owners must have air valves replaced free by dealers.
MazdaFeb 22, 2021 - Use cautionMedical device
Philips North America Llc recalls Incisive CT Computed Tomography X-ray System Model: 728143
Philips recalls Incisive CT Computed Tomography X-ray System Model 728143 due to risk of gantry tilting if actuators fail, potentially causing safety issues during use.
PhilipsFeb 22, 2021 - Lower riskMedical device
Mindray DS USA, Inc. dba Mindray North America recalls Mindray BeneVision Distributed Monitoring System( DMS) 1. p/n 115-051209-00 2. p/n 115-034414-00 and 115-034413-00 when
Mindray BeneVision Distributed Monitoring System (DMS) with specific software versions may freeze, causing patients to lose monitoring data. Affected units include models 115-051209-00 and 115-034414-00/115-034413-00 with software versions 03.04.00 through 04.04.01.
MindrayFeb 22, 2021 - Lower riskMedical device
RAYSEARCH LABORATORIES AB recalls RayStation 4.5, 4.7, 4.9, 5, 6, 7, 8A, 8B, 9A, 9B, 10A, 10B, RayPlan 1, 2, 7, 8A, 8B, 9A, 10A, 10B including some of
RaySearch recalls specific versions of RayStation and RayPlan software due to potential dose labeling errors when merging clinical beams. Affected versions include 4.5 to 10.1 with certain service packs. No immediate action is required but users should check their software version.
RaySearchFeb 22, 2021 - Lower riskMedical device
Sirtex Medical Limited recalls SIROS D-Vial Prep Set, Product Code SIR-10200 - Product Usage: intended for single use.
Sirtex recalls SIROS D-Vial Prep Set (product code SIR-10200) due to potential particulate matter in the D-Vial. This single-use medical device may pose a risk if used improperly.
SirtexFeb 22, 2021 - Lower riskMedical device
DePuy Orthopaedics, Inc. recalls ATTUNE¿ FIXED BEARING KNEE - Product Usage: composed of individually packaged femoral, tibial and patellar components
DePuy recalls specific lots of ATTUNE fixed bearing knee implants due to potential damaged packaging. These components are used in total knee replacements and may pose risks during surgical procedures.
DePuyFeb 22, 2021 - Lower riskMedical device
EPIX THERAPEUTICS, INC recalls EPIX Therapeutics DiamondTemp Bidrectional Large Curve Ablation Catheter, 7.5 French Size(2.48 mm), Connector Type: ODU
EPIX Therapeutics recalls DiamondTemp Bidrectional Large Curve Ablation Catheters due to incorrect size labeling on packaging and instructions, which may cause blood stagnation or clots.
EPIX TherapeuticsFeb 22, 2021 - Lower riskMedical device
Angiodynamics Inc. (Navilyst Medical Inc.) recalls AngioDynamics Safe Sheath Ultralite - Vascular Introducer/Catheter Introducer Catalogue #: VI10 - Product Usage: For
Angiodynamics recalls specific batch of Safe Sheath Ultralite vascular introducers due to potential sterility compromise. Affected units have Catalogue # VI10 and Lot # DP-11759. Contact for remedy.
AngiodynamicsFeb 22, 2021 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Cequa (cyclosporine ophthalmic solution) 0.09%, 60 Single-Use Vials (6 pouches x 10 single-use vials (0.25 mL each)),
Sun Pharma recalls Cequa (cyclosporine ophthalmic solution) 0.09% due to subpotent risk. This medication is for prescription use only and may not be as effective as intended.
Sun PharmaFeb 22, 2021 - Lower riskMeat & poultry
AH Company International Distribution, Inc., Recalls Pork Products Imported Without the Benefit of Inspection
USDA recalls 30,081 pounds of pork products imported without FSIS inspection. Consumers urged not to consume these items.
AH Company International DistributionFeb 19, 2021 - Use cautionVehicle
VOLVO VNL (2022) recall — Wheels
Volvo recalls 2022 VNL trucks with Alcoa Mirror Polish wheels for potential wheel failure causing crashes. Affected vehicles may need wheel replacement.
Volvo TrucksFeb 19, 2021 - Use cautionVehicle
BMW 530E (2020) recall — Back Over Prevention
BMW recalls 2020 530E models with potential rearview camera image issues that could increase crash risk. Owners must update software free of charge by April 2021.
BMWFeb 19, 2021 - Use cautionMedical device
Aesculap Implant Systems LLC recalls Universal Robot UR5 arm, PV010204 subcomponent of Aesculap Aeos Digital Microscope System, PV010
Aesculap recalls Universal Robot UR5 arm (PV010204) for potential robotic arm malfunction causing system restarts. Affected units have specific UDI-DI and serial numbers.
AesculapFeb 19, 2021 - Lower riskDrug
Noven Pharmaceuticals Inc recalls Daytrana (methylphenidate transdermal system) Delivers 30 mg over 9 hours (3.3 mg/hr) Contains: 30 Patches in a
Noven Pharmaceuticals recalls Daytrana patches due to defective delivery system. Out of specification mechanical peel may cause inconsistent medication release. Affected lots from 87377 to 88939 expiring 3/2021 to 8/2021.
NovenFeb 19, 2021 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Atorvastatin Calcium Tablets, 40mg, packaged in a) 90-count bottles, NDC 55111-123-90; b) 500-count bottles, NDC
Dr. Reddy's recalls 40mg Atorvastatin Calcium Tablets due to impurities that could pose health risks. Affected products include 90-count and 500-count bottles with specific NDC numbers. Consumers should check labels and contact the manufacturer for details.
Dr. Reddy'sFeb 19, 2021
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