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Vehicle Safety

Vehicle Recalls320,000+ NHTSA safety recalls Browse VehiclesEvery make, model and year Complaints2.1M+ consumer safety complaints TSBs4.7M technical service bulletins VIN LookupDecode any vehicle VIN instantly OBD Codes12,000+ diagnostic trouble codes Fuel EconomyEPA MPG data for all vehicles Safety Ratings11,700+ NHTSA crash test ratings Investigations5,300+ NHTSA defect investigations StatisticsRecall trends & safety analysis Compare VehiclesTwo vehicles side by side

Consumer Safety

Product Safety9,700+ CPSC product recalls Food Safety28,600+ FDA food recalls Pet Safety1.3M FDA animal adverse events Drug Safety17,500+ FDA drug recalls Device Safety38,400+ FDA device recalls Workplace Safety102,900+ OSHA injury reports Brand HistoryRecall lookup by company

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Bridge Safety624,000 bridge inspections Aviation Safety30,000+ NTSB aviation events Dam Safety92,600 dam safety records Water Safety433,000+ public water systems Railroad Safety438,000+ rail crossings Pipeline Safety8,800+ pipeline incidents State DashboardsSafety grades for all 50 states ZIP ReportAny 5-digit ZIP across 9 datasets

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Browse Device Recalls

184 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 184 FDA medical device recall enforcement actions. Each entry includes the device description, reason for recall, classification (Class I through III based on severity), recalling firm, and distribution details. Use the filters below to search by year, classification, state, or keyword.

Medical Device Recalls

Browse 184 FDA device recalls.

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DateProductReasonClassFirm
Nov 9, 2017 1. AutoPlex System, Product Number: 0605-887-000, UDI: (01)4546540593108; 2. ... Lack of sterility assurance as bioburden levels were found to be higher than internal acceptable ... Class II Stryker Instruments Div. of Stryker Corporation
Nov 9, 2017 Break-Away Femoral Nozzle, Product Number: 0206-512-000, UDI: (01)45465400394... Lack of sterility assurance as bioburden levels were found to be higher than internal acceptable ... Class II Stryker Instruments Div. of Stryker Corporation
Nov 9, 2017 1. Femoral Canal Pressurizer without Hub, Medium, Blue, Product Number: 0206-... Lack of sterility assurance as bioburden levels were found to be higher than internal acceptable ... Class II Stryker Instruments Div. of Stryker Corporation
Nov 9, 2017 Advanced Cement Mixing (ACM) Kit w/ Femoral Breakaway Nozzle & Prox. Med. Pre... Lack of sterility assurance as bioburden levels were found to be higher than internal acceptable ... Class II Stryker Instruments Div. of Stryker Corporation
Nov 9, 2017 1. 11g/10mm iVAS System Kit, Product Number: 0705-310-000, UDI: (01)761325250... Lack of sterility assurance as bioburden levels were found to be higher than internal acceptable ... Class II Stryker Instruments Div. of Stryker Corporation
Nov 9, 2017 10g/15mm (15/2) iVAS System Kit, Product Number: 0705-115-000, UDI: (01)76132... Lack of sterility assurance as bioburden levels were found to be higher than internal acceptable ... Class II Stryker Instruments Div. of Stryker Corporation
Nov 9, 2017 11g Verteport Cement Cannula (18/pkg), Product Number: 0306-511-000, UDI: (01... Lack of sterility assurance as bioburden levels were found to be higher than internal acceptable ... Class II Stryker Instruments Div. of Stryker Corporation
Nov 9, 2017 PCD Kit: Long 90, 13g Match-Ground w/ Bevel, Product Number: 0506-485-000, UD... Lack of sterility assurance as bioburden levels were found to be higher than internal acceptable ... Class II Stryker Instruments Div. of Stryker Corporation
Nov 9, 2017 Intramedullary Brush Standard O.D. 14 mm, Product Number: 6198-001-514, UDI: ... Lack of sterility assurance as bioburden levels were found to be higher than internal acceptable ... Class II Stryker Instruments Div. of Stryker Corporation
Nov 9, 2017 Revolution CMS w/ Femoral Breakaway Nozzle & Med. Press., Product Number: 060... Lack of sterility assurance as bioburden levels were found to be higher than internal acceptable ... Class II Stryker Instruments Div. of Stryker Corporation
Oct 16, 2017 The Stryker Thoracic Pedicle Feeler 6002-350-000 is a smart instrument for re... Stryker Instruments and Stryker Leibinger GmbH & Co. KG are voluntarily recalling certain serial... Class II Stryker Instruments Div. of Stryker Corporation
Mar 10, 2017 Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is a ... Product shipped proximate to or past the expiration date listed on the product label. Class II Stryker Instruments Div. of Stryker Corporation
Feb 28, 2017 Stryker SmartLife Large Aseptic Housing (7126-120-000) Stryker Instruments issued a notice of correction for an update to cleaning practices for the Str... Class II Stryker Instruments Div. of Stryker Corporation
Nov 30, 2016 8450-009-040 4.0MM Precision Round, 13CM, single use, Sterile The Stryker MI... Stryker Instruments is voluntarily recalling specific lots of sterile MIS Toolsteel Burs because ... Class II Stryker Instruments Div. of Stryker Corporation
Nov 30, 2016 8450-107-525 2.5MM Precision Match Head, 13CM, single use, Sterile The Stryk... Stryker Instruments is voluntarily recalling specific lots of sterile MIS Toolsteel Burs because ... Class II Stryker Instruments Div. of Stryker Corporation
Nov 30, 2016 8450-009-030 3.0MM Precision Round, 13CM, single use, Sterile The Stryker MI... Stryker Instruments is voluntarily recalling specific lots of sterile MIS Toolsteel Burs because ... Class II Stryker Instruments Div. of Stryker Corporation
Nov 30, 2016 8450-010-040 4.0MM Round, 13CM, single use, Sterile The Stryker MIS (Minim... Stryker Instruments is voluntarily recalling specific lots of sterile MIS Toolsteel Burs because ... Class II Stryker Instruments Div. of Stryker Corporation
Nov 30, 2016 8470-009-030 3.0MM Precision Round, 16CM, single use, Sterile The Stryker MI... Stryker Instruments is voluntarily recalling specific lots of sterile MIS Toolsteel Burs because ... Class II Stryker Instruments Div. of Stryker Corporation
Nov 30, 2016 8450-107-530 3.0MM Precision Match Head, 13CM, single use, Sterile The Stryk... Stryker Instruments is voluntarily recalling specific lots of sterile MIS Toolsteel Burs because ... Class II Stryker Instruments Div. of Stryker Corporation
Nov 30, 2016 8470-009-040 4.0MM Precision Round, 16CM, single use, Sterile The Stryker MI... Stryker Instruments is voluntarily recalling specific lots of sterile MIS Toolsteel Burs because ... Class II Stryker Instruments Div. of Stryker Corporation
Oct 11, 2016 RF MultiGen¿, 0406-900-000; Refurb RF MultiGen¿, 0406-900-000U Stryker Instruments is voluntarily recalling the Care Instructions/Instructions for Use packaged ... Class III Stryker Instruments Div. of Stryker Corporation
Aug 17, 2016 Sagittal Blade 18.0X0.97X90MM, Model Number: 6118-097-090 Product Usage: ... Stryker Instruments is voluntarily recalling the Sagittal Blade 18.0X.97X90MM due to the potentia... Class II Stryker Instruments Div. of Stryker Corporation
Jul 1, 2016 120 V Neptune 3 Rover, Model Number: 0703-001-000 Stryker initiated a voluntary recall of the 120 V Neptune 3 Rover on 07/01/2016, due to a potent... Class II Stryker Instruments Div. of Stryker Corporation
Jun 24, 2016 2.3MM Tapered Router, Product Number 5407-FA2-023 A router is a cutting acc... A variation in flute depth on the routers was observed. The variation in flute depth may cause th... Class II Stryker Instruments Div. of Stryker Corporation
Jun 16, 2016 5.0mm Round Fluted Bur, Super Long Stryker Instruments initiated a voluntary recall of specific lots of Round Fluted Burs, due to ta... Class II Stryker Instruments Div. of Stryker Corporation
Jun 16, 2016 6.0mm Round Fluted Bur, Super Long Stryker Instruments initiated a voluntary recall of specific lots of Round Fluted Burs, due to ta... Class II Stryker Instruments Div. of Stryker Corporation
Jun 14, 2016 Stryker AutoPlex System. Model Numbers 0607-687-000, 0605-887-000, 0605-687... The Piston Head can become separated from the Delivery Piston, blocking the injection assembly Va... Class II Stryker Instruments Div. of Stryker Corporation
Apr 28, 2016 Maestro Air Motor Pneumatic cranial drill motor. The Maestro Air Pneumatic... Due to the buildup of grease within the hose and motor, the product may require multiple attempts... Class II Stryker Instruments Div. of Stryker Corporation
Mar 22, 2016 Spetzler Claw Tip, Universal - 5450-800-311 Spetzler Open Angle Micro Claw ... The Spetzler Claw Tip was packaged with the incorrect Tip Sleeve Assembly. The Tip Sleeve Assembl... Class II Stryker Instruments Div. of Stryker Corporation
Mar 21, 2016 SurgiCounter scanner, part of the SurgiCount Safety-Sponge System. Model nu... The affected scanner does not correctly interact with the SC360 software. When docked pre/postope... Class II Stryker Instruments Div. of Stryker Corporation
Feb 4, 2016 50001 (Inrad) AccuPlace Drace Stereotaxic Needle Guide; Assists the user wit... During an evaluation of the product packaging, it was determined that there is a potential for th... Class II Stryker Instruments Div. of Stryker Corporation
Feb 4, 2016 50000 (Inrad) AccuPlace Drace Stereotaxic Needle Guide; Assists the user wit... During an evaluation of the product packaging, it was determined that there is a potential for th... Class II Stryker Instruments Div. of Stryker Corporation
Feb 4, 2016 (Stryker) AccuPlace Straight Level Needle Guide; Assists the user with insert... During an evaluation of the product packaging, it was determined that there is a potential for th... Class II Stryker Instruments Div. of Stryker Corporation
Feb 4, 2016 (Stryker) AccuPlace Round Level Needle Guide; Assists the user with inserting... During an evaluation of the product packaging, it was determined that there is a potential for th... Class II Stryker Instruments Div. of Stryker Corporation
Nov 23, 2015 Cournand Modified 2-PC 19G, 5.4cm or (Guidewire Introducer Needle) 20 units ... The Guidewire Introducer Needle (0910-192-000) was shipped after the documented expiration date o... Class II Stryker Instruments Div. of Stryker Corporation
Jul 20, 2015 Neptune 2 Waste Management System Docking Station (120V and 230V), New and Re... The Fluid Coupling Sleeve, a component within the Neptune Waste Management System Docker, may be ... Class II Stryker Instruments Div. of Stryker Corporation
Jun 2, 2015 Stryker SelectCore Variable Throw Biopsy Device, 14G, 10CM Product Usage: ... Stryker Instruments is recalling the Stryker SelectCore Variable Throw Biopsy Device due to the p... Class II Stryker Instruments Div. of Stryker Corporation
May 22, 2015 0702-001-350Q, Diverter Valve Assembly 0702-001-000, Neptune 2 Rover Ultra (... Stryker Instruments is initiating a recall of the Neptune 2 Waste Management System due to compla... Class II Stryker Instruments Div. of Stryker Corporation
May 8, 2015 0210-312-000-Woundcare Replacement kit with soft tip; 0210-318-000; Woundcare... Potential sterility breach in the packaging. Class II Stryker Instruments Div. of Stryker Corporation
May 4, 2015 Navigation System II-Cart, 7700-100-000 with Articulated Arm Camera, 7700-103... Stryker initiated a device recall of the Navigation System II-Cart, Camera Articulated Arm becaus... Class II Stryker Instruments Div. of Stryker Corporation
Apr 24, 2015 EliteCore Full Core Biopsy Device. EliteCore 18G, 20cm with and without HiLi... Potential for the device cannula to overthrow past the intended length. Class II Stryker Instruments Div. of Stryker Corporation
Mar 26, 2015 1/4 in. Round Drain with Trocar Curved Trocar with Wound Drain/Double Troc... Stryker Instruments is voluntarily recalling the CBCII Wound Drains and Ambulating Bulb for a pot... Class II Stryker Instruments Div. of Stryker Corporation
Mar 26, 2015 3/16 in. Curved Trocar with Wound Drain Curved Trocar with Wound Drain/Dou... Stryker Instruments is voluntarily recalling the CBCII Wound Drains and Ambulating Bulb for a pot... Class II Stryker Instruments Div. of Stryker Corporation
Mar 26, 2015 1/4 in. Double Trocar with Wound Drain Curved Trocar with Wound Drain/Doub... Stryker Instruments is voluntarily recalling the CBCII Wound Drains and Ambulating Bulb for a pot... Class II Stryker Instruments Div. of Stryker Corporation
Mar 26, 2015 Ambulating Bulb Ambulating Bulb: The Ambulating Bulb comprises four main c... Stryker Instruments is voluntarily recalling the CBCII Wound Drains and Ambulating Bulb for a pot... Class II Stryker Instruments Div. of Stryker Corporation
Mar 26, 2015 1/8 in. Curved Trocar with Wound Drain Curved Trocar with Wound Drain/Doub... Stryker Instruments is voluntarily recalling the CBCII Wound Drains and Ambulating Bulb for a pot... Class II Stryker Instruments Div. of Stryker Corporation
Mar 26, 2015 1/8 in. Trocar with Single Drain Curved Trocar with Wound Drain/Double Tro... Stryker Instruments is voluntarily recalling the CBCII Wound Drains and Ambulating Bulb for a pot... Class II Stryker Instruments Div. of Stryker Corporation
Mar 26, 2015 1/4 in. Curved Trocar with Wound Drain Curved Trocar with Wound Drain/Doub... Stryker Instruments is voluntarily recalling the CBCII Wound Drains and Ambulating Bulb for a pot... Class II Stryker Instruments Div. of Stryker Corporation
Mar 26, 2015 1/4 in. Trocar with Single Drain Curved Trocar with Wound Drain/Double Tro... Stryker Instruments is voluntarily recalling the CBCII Wound Drains and Ambulating Bulb for a pot... Class II Stryker Instruments Div. of Stryker Corporation
Mar 26, 2015 3/16 in. Trocar with Single Drain Curved Trocar with Wound Drain/Double Tr... Stryker Instruments is voluntarily recalling the CBCII Wound Drains and Ambulating Bulb for a pot... Class II Stryker Instruments Div. of Stryker Corporation

Frequently Asked Questions

When a device safety issue is identified, the manufacturer or FDA initiates a recall. The FDA publishes an enforcement report detailing the device, the reason for the recall, and distribution. Healthcare facilities and providers are notified to check their inventory and take corrective action.

All types — from simple devices like blood glucose test strips and surgical gloves to complex devices like pacemakers, defibrillators, insulin pumps, hip implants, and ventilators. Software-driven devices are increasingly common in recalls due to bugs and cybersecurity vulnerabilities.

Use the search and filter tools on this page. Each recall entry includes the device description, model numbers, and distribution details so you can determine if your device is affected. Contact your healthcare provider if you find a match.