Stryker Neurovascular recalls

Stryker Neurovascular has 109 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 1 Jul 2026. 15 are still ongoing. 1 was reported in the last 12 months.

Total recalls109since 2013
Last 12 months1reported
Class I11% of total
Ongoing15latest 1 Jul 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 1 1%Class II 108 99%Class III 0 0%

Why stryker neurovascular is recalled

By year

Ongoing stryker neurovascular recalls

15 active

All stryker neurovascular recalls, newest first

109 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIInzone Detachment System recalled by Stryker NeurovascularStryker NeurovascularDevice MalfunctionNationwide
DeviceCLASS IIThe Trevo Trak 21 Microcatheter is a single-lumen recalledStryker NeurovascularPackaging DefectsNationwide
DeviceCLASS IIThe Synchro Neuro Guidewires are a steerable guidewire recalledStryker NeurovascularOtherNationwide
DeviceCLASS IIThe Synchro Select Guidewires are a steerable guidewire recalledStryker NeurovascularOtherNationwide
DeviceCLASS IIThe Synchro2 Guidewires are a steerable guidewire family recalledStryker NeurovascularOtherNationwide
DeviceCLASS IITrevo Pro 14 Microcatheter recalled by Stryker NeurovascularStryker NeurovascularSterilityNationwide
DeviceCLASS IIFlowGate2 8F recalled by Stryker NeurovascularStryker NeurovascularSterilityNationwide
DeviceCLASS IITrevo XP ProVue Retriever recalled by Stryker NeurovascularStryker NeurovascularSterilityNationwide
DeviceCLASS IITrevo NXT ProVue , US recalled by Stryker NeurovascularStryker NeurovascularSterilityNationwide
DeviceCLASS IIDAC 044 115cm, Catalog recalled by Stryker NeurovascularStryker NeurovascularSterilityNationwide
DeviceCLASS IISynchro .014"guide wire tip recalled by Stryker NeurovascularStryker NeurovascularSterilityNationwide
DeviceCLASS IITrevo Trak 21 Microcatheter recalled by Stryker NeurovascularStryker NeurovascularSterilityNationwide
DeviceCLASS IITrevo ProVue recalled by Stryker NeurovascularStryker NeurovascularSterilityNationwide
DeviceCLASS IIThe Distal Access Catheter is a single-lumen, braided shaft recalledStryker NeurovascularOtherNationwide
DeviceCLASS IITrevo Trak 21 Microcatheter recalled by Stryker NeurovascularStryker NeurovascularOtherNationwide
DeviceCLASS ITrevo XP ProVue Retriever recalled by Stryker NeurovascularStryker NeurovascularOther47 states
DeviceCLASS IIAXS Vecta 74 Aspiration Catheter recalled by Stryker NeurovascularStryker NeurovascularPackaging DefectsNationwide
DeviceCLASS IIAXS Vecta 71 Aspiration Catheter recalled by Stryker NeurovascularStryker NeurovascularPackaging DefectsNationwide
DeviceCLASS IISynchro2, Soft Pre-shaped Guidewire recalled by Stryker NeurovascularStryker NeurovascularOtherNationwide
DeviceCLASS IISynchro2 SOFT Guidewire with Hydrophilic Coating recalledStryker NeurovascularOtherNationwide
DeviceCLASS IISynchro2 Standard Pre-shaped Guidewire recalled by Stryker NeurovascularStryker NeurovascularOtherNationwide
DeviceCLASS IISynchro2 Standard Guidewire recalled by Stryker NeurovascularStryker NeurovascularOtherNationwide
DeviceCLASS IISynchro2 Standard Pre-shaped Guidewire recalled by Stryker NeurovascularStryker NeurovascularOtherNationwide
DeviceCLASS IISynchro2 Standard Guidewire with Hydrophilic Coating recalledStryker NeurovascularOtherNationwide
DeviceCLASS IISynchro2, Soft Pre-shaped Guidewire recalled by Stryker NeurovascularStryker NeurovascularOtherNationwide
DeviceCLASS IISynchro2, SOFT Guidewire with Hydrophilic Coating recalledStryker NeurovascularOtherNationwide
DeviceCLASS IIMerci 9F, Balloon Guide Catheter recalled by Stryker NeurovascularStryker NeurovascularLabeling ErrorsCA
DeviceCLASS IIAXS Infinity LS Plus Long Sheath recalled by Stryker NeurovascularStryker NeurovascularPackaging DefectsNationwide
DeviceCLASS IIAxs Infinity LS Long Sheath:((6F/./ Gen recalledStryker NeurovascularOther6 states
DeviceCLASS IIWingspan Stent System recalled by Stryker NeurovascularStryker NeurovascularOtherCA

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.