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
35,004 found- Lower riskMedical device
Becton, Dickinson and Company, BD Biosciences recalls Analyte specific reagent. REF/UDI: 641408/641408-4012-1-1 (US); 641417/641417-1157-1-01 (OUS); 641399/641399-4012-1-01
BD Biosciences recalls Analyte specific reagent due to false positive reactions. Affected units have REF/UDI codes listed. Users should stop using to avoid inaccurate test results.
BD BiosciencesMar 31, 2020 - Use cautionMedical device
Spectranetics Corporation recalls Bridge Occlusion Balloon, REF 590-001, QTY 1, Sheath Compatibility 12F, Guidewire Compatibility 0.035 in, Working
Spectranetics recalls Bridge Occlusion Balloon REF 590-001 due to potential blood clot formation if left in blood vessels too long. All users should minimize balloon time in vasculature to prevent embolization.
SpectraneticsMar 31, 2020 - UnratedDrug
Noven Therapeutics, LLC recalls Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr), 30-count box, Rx only,
Noven Therapeutics recalls Daytrana (methylphenidate transdermal system) 30-count boxes due to defective delivery system causing inconsistent dosing. No remedy specified in official notice.
Noven TherapeuticsMar 31, 2020 - Stop using nowVehicle
NISSAN ARMADA (2015) recall — Air Bags
Nissan is recalling 2015 Armada models due to air bag inflator rupture risk causing serious injury or death. Owners must have inflators replaced free by May 2020.
NissanMar 30, 2020 - Use cautionVehicle
ALTEC AT200A (2018) recall — Tires
Altec recalls 2016-2018 AT200A vehicles with potentially incorrect rear tire sizes/load ratings that could cause overload and crash risk. Owners get free tire replacement.
AltecMar 30, 2020 - Use cautionMedical device
Elekta Inc recalls Leksell Vantage Stereotactic System. Instrument Carrier, Part of Leksell Vantage Arc (1053958). Neurological
Elekta recalls Leksell Vantage Stereotactic System Instrument Carrier (serial numbers SH00106 to SH00178) due to a faulty locking piece that may not secure properly to the Arc system.
ElektaMar 30, 2020 - Stop using nowMedical device
Beckman Coulter Inc. recalls iChem¿VELOCITY Urine Chemistry System-
Beckman Coulter recalls iChem¿VELOCITY Urine Chemistry Systems with a defect in the SATA power adapter cable that could cause charring, melting, smoke, or fire. Affected models include catalog numbers 700-7176-001 and 700-7177-001.
Beckman CoulterMar 30, 2020 - Lower riskMedical device
Boston Scientific Corporation recalls MoXy Laser Fiber, Material Number 0010-2400 - Product Usage: The fiber can be used for the surgical incision/excision,
Boston Scientific recalls MoXy Laser Fiber (Material Number 0010-2400) due to potential metal cap and fiber tip breakage during use. Affected units have specific lot numbers listed in the recall notice.
Boston ScientificMar 30, 2020 - UnratedDrug
Par Pharmaceutical Inc. recalls Glycopyrrolate Tablets, USP 1 mg, 100-count bottle, Rx only, Dist. by: Par Pharmaceutical, Chestnut Ridge, NY, 10977,
Par Pharmaceutical recalls 100-count Glycopyrrolate Tablets (1mg) due to unknown impurities. Rx-only medication with NDC 49884-0065-01 and lot #32809101. No specific action steps listed in recall notice.
Par PharmaceuticalMar 30, 2020 - Use cautionVehicle
CAN-AM SPYDER RT (2020) recall — Service Brakes, Hydraulic
BRP recalls 2020 Can-Am Spyder RT motorcycles with potential brake failure during emergency stops. Owners must contact BRP for free bracket installation by April 2020.
Can-AmMar 27, 2020 - Use cautionMedical device
Stryker Sustainability Solutions recalls Cardiovascular Reprocessed ViewFlex Xtra ICE Catheter, REF D087031, OM St. Jude Medical, Size 9F (3.2mm), Length 90 cm,
Stryker recalls certain Cardiovascular Reprocessed ViewFlex Xtra ICE Catheters with incorrect expiration dates that may cause sterility breaches or treatment delays. Affected units have a one-year shelf life but are labeled as two years.
StrykerMar 27, 2020 - Lower riskMedical device
Edwards Lifesciences, LLC recalls Sterile Oxymetry Oligon Catheter Kit. Pressure injectable. REF/UDI:XA3816SAFKT/ (01)00690103197181
Edwards Lifesciences recalls Sterile Oxymetry Oligon Catheter Kit (model XA3816SFKT) due to compromised packaging. Affected units have specific lot codes. Consumers should check their kit for packaging issues.
Edwards LifesciencesMar 27, 2020 - Lower riskFood
CT Health Solutions, LLC recalls We Like Vitamins, Lycopene 50 mg, Dietary Supplement, 200 Capsules
CT Health Solutions recalls We Like Vitamins Lycopene 50 mg due to low potency. Check lot #02121902 for details.
We Like VitaminsMar 27, 2020 - Use cautionVehicle
BMW 328D (2015) recall — Power Train
BMW recalls 2015 328D models with potential rear wheel power loss causing crashes. Owners must have transfer case inspected and repaired free by dealers.
BMWMar 26, 2020 - Use cautionVehicle
FREIGHTLINER SPRINTER 4500 (2019) recall — Equipment
Daimler Vans USA recalls 2019 Freightliner Sprinter 4500 vehicles with incorrect Auto-P function instructions in the Operator's Manual, risking rollaway and crashes.
FreightlinerMar 26, 2020 - Use cautionVehicle
DODGE DURANGO (2019) recall — Power Train
Chrysler recalls certain 2019 Dodge Durango vehicles with potential power loss or transmission park function failure due to worn differential gears. Affected owners should contact Chrysler for free front differential replacement.
ChryslerMar 26, 2020 - Use cautionVehicle
CHEVROLET BOLT EV (2020) recall — Latches/Locks/Linkages
Chevrolet is recalling 2020 Bolt EVs with rear door handle cable issues that could cause doors to open while driving, risking passenger injury. Owners must contact GM for free repairs.
ChevroletMar 26, 2020 - Use cautionMedical device
Becton Dickinson & Company recalls CareFusion Safe-T-Centesis Catheter Drainage Tray, Sterile, For Single Use Only, Rx only, Catalog Number PIG1280T, UDI
Becton Dickinson recalls sterile catheter drainage trays with wrong needle size. This may cause injury during medical procedures. Affected units have specific catalog and lot numbers.
Becton DickinsonMar 26, 2020 - Lower riskMedical device
Stryker Instruments Div. of Stryker Corporation recalls Neptune E-SEP 165mm Blade Electrode, Catalog Number 0703-165-001 - Product Usage: The Neptune E-SEP is an Integrated
Stryker recalls Neptune E-SEP 165mm Blade Electrode (Lot 16240231) due to expired product from a distribution error. This may not affect safety but requires checking the lot number.
StrykerMar 26, 2020 - UnratedMedical device
Gentell, Inc recalls Gentell Honey Hydrogel 2"x2" Saturated Gauze- A hydrating wound dressing containing hydrogel and honey (100%
Gentell recalls 100% honey wound dressings due to improper FDA registration. Affected products include specific model numbers and lot ranges. Consumers should contact the company for details.
GentellMar 26, 2020 - Lower riskMedical device
Medtronic Sofamor Danek USA Inc recalls VERTEX SELECT MULTI AXIAL SCREW. 4.0 X 38MM MULTI AXIAL SCREW. Lot H5517628
Medtronic Sofamor Danek recalls Vertex Select Multi Axial Screws (4.0 x 38mm) with shorter length than labeled. Affected units may not fit properly in spinal surgery.
Medtronic Sofamor DanekMar 26, 2020 - Lower riskMedical device
Shanghai United Imaging Healthcare Co., Ltd. recalls Positron Emission Tomography and Computed Tomography System, Model: uMI 550, Material Number: 88000057 - Product Usage:
Shanghai United Imaging Healthcare recalls uMI 550 CT scanners with specific software versions due to potential image display issues during bolus tracking. Affected units may require manual scanning, risking patient rescan. Contact for remedy details.
Shanghai United Imaging HealthcareMar 26, 2020 - Stop using nowDrug
Avet Pharmaceuticals, Inc. recalls Losartan Potassium Tablets USP 100 mg, supplied in a) 30 count (NDC 23155-646-03, b) 90 count (NDC 23155-646-09) and
FDA-confirmed impurity in Avet Losartan Potassium Tablets 100mg may exceed safe levels. Recalled 30-count and 90-count bottles. Stop using immediately.
Avet PharmaceuticalsMar 26, 2020 - Lower riskDrug
Innovative Intrathecal Solutions, Inc. dba Innovative Compounding Pharmacy recalls Testosterone Cypionate In Sesame Oil 200mg/ml, 5 mL, Injectable, Rx only, INNOVATIVE COMPOUNDING PHARMACY, 41536
Innovative Compounding Pharmacy recalls testosterone cypionate injections due to lack of sterility assurance. Affected lots expire by April 2020. Contact for details.
Innovative Compounding PharmacyMar 26, 2020 - Use cautionFood
MIN JIANG FOOD STORE INC DBA KOI KOI TRADING recalls Fresh Salmon; Brand names : Bakka, Superior, Scottish Canada, Ocean Quality, Norway. Refrigerate Unit size: 10-12 lbs.,
MIN JIANG FOOD STORE INC DBA KO: Koi Koi Trading recalls fresh salmon products (Bakka, Superior, etc.) due to potential Listeria monocytogenes contamination. Consumers should check product labels for size and refrigeration instructions.
Koi Koi TradingMar 26, 2020 - Use cautionVehicle
GILLIG LOW FLOOR (2019) recall — Electrical System
Gillig is recalling certain 2012-2020 Low Floor buses due to potential electrical short circuits that could cause fire. Owners must have circuit breakers replaced free by dealers.
GilligMar 25, 2020 - Stop using nowVehicle
FREIGHTLINER SPRINTER 4500 (2019) recall — Service Brakes, Air
Daimler Vans USA recalls certain 2019 Freightliner Sprinter vehicles due to brake hose chafing. Dealers will inspect and replace hoses free of charge.
Freightliner SprinterMar 25, 2020 - Use cautionVehicle
THOR MOTOR COACH AXIS (2020) recall — Power Train
Thor Motor Coach is recalling certain 2020 Axis motorhomes due to potential rear axle fluid issues that could cause driveshaft separation or unintended vehicle movement if the parking brake isn't applied.
Thor Motor CoachMar 25, 2020 - Use cautionVehicle
INDIAN CHALLENGER (2020) recall — Engine
Indian recalls 2020 Challenger motorcycles with potential engine power loss due to output shaft bearing failure. Owners with less than 50 miles on odometer should stop using until repaired.
IndianMar 25, 2020 - Lower riskMedical device
Abbott Vascular recalls Xience Sierra TM Everolimus Eluting Coronary Stent System, RX 3.5mm x 33mmStrength: 100 ¿g/cm¿, Nominal Everolimus
Abbott recalls Xience Sierra Everolimus stents with incorrect expiration dates. Affected stents may be unsafe for use. Contact Abbott for details.
Abbott VascularMar 25, 2020
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