Stryker recalls

Stryker has 192 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 12 Aug 2026. 108 are still ongoing. 18 were reported in the last 12 months.

Total recalls192since 2016
Last 12 months18reported
Class I00% of total
Ongoing108latest 12 Aug 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 192 100%Class III 0 0%

By year

Ongoing stryker recalls

108 active

All stryker recalls, newest first

192 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIPkg., Strykeflow Suction/irrigator Ps recalled by StrykerStrykerPackaging DefectsNationwide
DeviceCLASS IIAhto Tube Set With Tip Packaging recalled by StrykerStrykerPackaging DefectsNationwide
DeviceCLASS IIPkg., Single Spike Tube Set recalled by StrykerStrykerPackaging DefectsNationwide
DeviceCLASS IIAhto Tube Set Packaging recalled by StrykerStrykerPackaging DefectsNationwide
DeviceCLASS IIAhto Dual Spike Tube Set Packaging recalled by StrykerStrykerPackaging DefectsNationwide
DeviceCLASS IIHoffmann II Connecting Rod Micro recalled by StrykerStrykerSterilityNationwide
DeviceCLASS IIHoffmann II Connecting Rod Micro recalled by StrykerStrykerSterilityNationwide
DeviceCLASS IIHoffmann II Connecting Rod Micro recalled by StrykerStrykerSterilityNationwide
DeviceCLASS IIHoffmann II Connecting Rod Micro recalled by StrykerStrykerSterilityNationwide
DeviceCLASS IIHoffmann II Connecting Rod Micro recalled by StrykerStrykerSterilityNationwide
DeviceCLASS IIHoffmann II Connecting Rod Micro recalled by StrykerStrykerSterilityNationwide
DeviceCLASS IIHoffmann II Connecting Rod Micro recalled by StrykerStrykerSterilityNationwide
DeviceCLASS IINeptune Smart Docking Station (120V) recalled by StrykerStrykerDevice MalfunctionNationwide
DeviceCLASS IIThermedx FluidSmart Urology Tube Set recalled by StrykerStrykerOtherNationwide
DeviceCLASS IIMolli 2 System includes: MM1000 (Pack recalled by StrykerStrykerOtherNationwide
DeviceCLASS IINICO Myriad Illumination Pack Product No. NN recalled by StrykerStrykerPackaging DefectsNationwide
DeviceCLASS IINN-8000 MHP recalled by StrykerStrykerPackaging DefectsNationwide
DeviceCLASS IINICO BrainPath recalled by StrykerStrykerPackaging DefectsNationwide
DeviceCLASS IISmartPump Tourniquet, disposable sterile recalled by StrykerStrykerPackaging DefectsNationwide
DeviceCLASS IIStryker, StrykeFlow , REF: 0250070500, 2, Disposable recalledStrykerPackaging DefectsNationwide
DeviceCLASS IIStryker, StrykeFlow REF: 0250070520 recalledStrykerPackaging DefectsNationwide
DeviceCLASS IIFemoral Nail, Right T2 GTN mm recalled by StrykerStrykerOtherNationwide
DeviceCLASS IILong Nail, Right Gamma4 10x320mm recalled by StrykerStrykerOtherNationwide
DeviceCLASS IIFemoral Nail, LEFT T2 GTN mm recalled by StrykerStrykerOtherNationwide
DeviceCLASS IIGuide Wire with Ruler Tube mm DIA recalled by StrykerStrykerForeign MaterialNationwide
DeviceCLASS IIGuide Wire with Ruler Tube mm DIA recalled by StrykerStrykerForeign MaterialNationwide
DeviceCLASS IINasopore Standard fragmentable nasal dressing recalled by StrykerStrykerSterilityNationwide
DeviceCLASS IIOtopore Cylinder Standard outer ear dressings recalled by StrykerStrykerSterilityNationwide
DeviceCLASS IINasopore fragmentable nasal dressing, Firm recalled by StrykerStrykerSterilityNationwide
DeviceCLASS IINasopore Ex Firm fragmentable nasal dressing recalled by StrykerStrykerSterilityNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.