Stryker Instruments Div. of Stryker recalls

Stryker Instruments Div. of Stryker has 161 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 27 Jul 2022.

Total recalls161since 2012
Last 12 months0reported
Class I42% of total
Ongoing0latest 27 Jul 2022

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 4 2%Class II 153 95%Class III 4 2%

Why stryker instruments div. of stryker is recalled

By year

All stryker instruments div. of stryker recalls, newest first

161 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIITriton Sponge System recalled by Stryker Instruments Div. ofStryker Instruments Div. of StrykerDevice MalfunctionNationwide
DeviceCLASS IITriton Canister System (finished part numbers FG recalledStryker Instruments Div. of StrykerDevice MalfunctionNationwide
DeviceCLASS IISurgiCount+ System Application recalled by Stryker Instruments Div. ofStryker Instruments Div. of StrykerDevice MalfunctionKS, ME
DeviceCLASS IIStryker Zyphr Disposable Cranial Perforator recalledStryker Instruments Div. of StrykerForeign MaterialNationwide
DeviceCLASS IINeptune E-sep Blade Electrode recalled by Stryker Instruments Div. ofStryker Instruments Div. of StrykerOtherMI
DeviceCLASS IITelescopic Smoke Evac Pencil, PB, Coated, Product No. Shktspcl recalledStryker Instruments Div. of StrykerOtherNationwide
DeviceCLASS IITelescopic Uncoated (Push Button), Product No. SHK TSPL recalledStryker Instruments Div. of StrykerOtherNationwide
DeviceCLASS IISafeAir Telescopic Smoke Evacuation Pencil, Product No. recalledStryker Instruments Div. of StrykerOtherNationwide
DeviceCLASS IIColor Cuff Disposable Tourniquet Cuff X, 1BLA recalledStryker Instruments Div. of StrykerPackaging DefectsNationwide
DeviceCLASS IIColor Cuff Disposable Tourniquet Cuff X, 1BLA recalledStryker Instruments Div. of StrykerPackaging DefectsNationwide
DeviceCLASS IIC2 Nerve Monitor, 4 Channel recalled by Stryker Instruments Div. ofStryker Instruments Div. of StrykerDevice MalfunctionNationwide
DeviceCLASS IIC2 Nerve Monitor, 8 Channel recalled by Stryker Instruments Div. ofStryker Instruments Div. of StrykerDevice MalfunctionNationwide
DeviceCLASS IIPerformance Series Sagittal Blade recalledStryker Instruments Div. of StrykerSterilityNationwide
DeviceCLASS IIT5 Zipper Toga with Peel-Away Face Shield, (L/XL) recalledStryker Instruments Div. of StrykerOtherNationwide
DeviceCLASS IIT4 Pullover Toga, Large recalled by Stryker Instruments Div. ofStryker Instruments Div. of StrykerOtherNationwide
DeviceCLASS IIT4 Pullover Toga, Regular recalled by Stryker Instruments Div. ofStryker Instruments Div. of StrykerOtherNationwide
DeviceCLASS IIT4 Pullover Toga, (S/M) recalled by Stryker Instruments Div. ofStryker Instruments Div. of StrykerOtherNationwide
DeviceCLASS IIT4 Pullover Toga, X-Large recalled by Stryker Instruments Div. ofStryker Instruments Div. of StrykerOtherNationwide
DeviceCLASS IIT4 Zipper Toga, (L/XL) recalled by Stryker Instruments Div. ofStryker Instruments Div. of StrykerOtherNationwide
DeviceCLASS IIT4 Zipper Toga, Regular recalled by Stryker Instruments Div. ofStryker Instruments Div. of StrykerOtherNationwide
DeviceCLASS IIT4 Pullover Toga, L/XL recalled by Stryker Instruments Div. ofStryker Instruments Div. of StrykerOtherNationwide
DeviceCLASS IIT5 Zipper Toga with Peel-Away Face Shield, (XL/T) recalledStryker Instruments Div. of StrykerOtherNationwide
DeviceCLASS IIT4 Zipper Toga, X-Large recalled by Stryker Instruments Div. ofStryker Instruments Div. of StrykerOtherNationwide
DeviceCLASS IIT4 Zipper Toga (S/M) recalled by Stryker Instruments Div. ofStryker Instruments Div. of StrykerOtherNationwide
DeviceCLASS IICement Cartridge with Breakaway Femoral Nozzle recalledStryker Instruments Div. of StrykerSterilityDC
DeviceCLASS IIInterPulse Handpiece with coaxial bone cleaning tip recalledStryker Instruments Div. of StrykerSterilityDC
DeviceCLASS IIRevolution 90 Degree Tibial Nozzle, Product Number recalledStryker Instruments Div. of StrykerSterilityDC
DeviceCLASS IIThe Stryker Thoracic Pedicle Feeler 6002-350-000 is a smart recalledStryker Instruments Div. of StrykerPotency & AssayMI
DeviceCLASS IIAutoPlex System, Product Number recalled by Stryker Instruments Div. ofStryker Instruments Div. of StrykerSterilityDC
DeviceCLASS IIBreak-Away Femoral Nozzle, Product Number recalledStryker Instruments Div. of StrykerSterilityDC

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.