Every recall we track for Stryker Neurovascular — 39 in all — plus the complaints and injury reports the public filed about them.
Stryker recalls INZONE Detachment System devices with premature battery drain causing failure to power on or detach coils, potentially requiring medical intervention.
Stryker Neurovascular recalls Trevo Trak 21 Microcatheters with Out of US approved instructions distributed in the US. No immediate action needed as the error is a distribution mistake, not a safety issue.
Stryker recalls Trevo Pro 14 and 18 Microcatheters due to potential endotoxin levels exceeding safety standards, which may cause fever, shock, or meningitis.
Stryker recalls FlowGate2 8F catheters (catalogs 90485/90495) due to potential endotoxin levels exceeding safety limits, which may cause fever, shock, or meningitis. Affected units include specific lot numbers.
Stryker Neurovascular recalls specific Trevo XP ProVue Retriever models due to potential endotoxin levels exceeding safety standards, which may cause fever, shock, or aseptic meningitis.
Stryker recalls certain Trevo NXT ProVue 3x32 kits that may have high endotoxin levels, increasing risk of fever, shock, or aseptic meningitis. Affected kits include specific catalog numbers and lot codes.
Stryker Neurovascular recalls DAC 044 115cm devices (Catalog 90760) due to potential endotoxin levels exceeding safety limits, which may cause fever, shock, or meningitis.
Stryker recalls certain Synchro guide wires due to potential endotoxin levels exceeding safety standards, which could increase risk of fever, shock, or aseptic meningitis.
Stryker recalls Trevo Trak 21 Microcatheter (Catalog 90338) due to potential endotoxin levels exceeding safety standards, which may cause fever, shock, or meningitis. Affected units include specific lots and serial numbers.
Stryker recalls Trevo ProVue devices (Catalog: 90184) that may have high endotoxin levels, increasing risk of fever, shock, or aseptic meningitis. Affected units include specific lots and UDI-DI numbers.
Stryker recalls certain Synchro Neuro Guidewires with PTFE coating damage risk when backloaded through older introducer accessories. Affected lots include specific serial numbers listed in the recall.
Stryker Neurovascular recalls certain Synchro SELECT Guidewires with older introducer accessories that may cause PTFE coating damage when backloaded during use. Affected lots have sharper edges that can peel off the coating.
Stryker Neurovascular recalls Synchro2 Guidewires with certain lots due to PTFE coating damage when backloading through older introducer accessories. Affected units have specific lot numbers listed in the recall.
Stryker Neurovascular recalls Distal Access Catheter (Lot #0000486382) due to out-of-specification endotoxin results. Affected units may pose a risk of infection or adverse reactions. Consumers should contact Stryker for details.
Stryker recalls specific Trevo Trak 21 Microcatheter models due to missing product drawing on carton labels. This may affect medical device safety during procedures.
Stryker recalls specific models of Trevo XP ProVue Retriever due to increased risk of stent retriever separation from core wire during procedures, potentially leaving devices in vasculature. Affected units include certain sizes and reference numbers.
Stryker Neurovascular recalls AXS Infinity LS Plus Long Sheath (70cm, 80cm, 90cm) due to brittle catheter shaft that may fracture during use. Affected medical devices sold in the US.
Stryker Neurovascular recalls AXS Vecta 74 Aspiration Catheters (Catalog # INC-11597-115, 125, 132) due to potential breakage or kinking if improperly handled. These catheters are used for stroke treatment and must be handled carefully to avoid injury.
Stryker Neurovascular recalls AXS Vecta 71 Aspiration Catheters (Catalog # INC-11129-115, 125, 132) due to potential breakage or kinking if improperly removed from packaging or during use. Affected units have a use-by date of 2021-11-29.
Stryker Neurovascular recalls 9F Balloon Guide Catheters due to labeling error where 8F catheters were packaged with 9F. This affects specific lot numbers sold outside the US. No action needed as the product was not distributed in the US.
Stryker recalls Synchro2 guidewires with incorrect outer diameter label (0.036mm instead of 0.36mm). This could lead to improper use during medical procedures. Affected units have specific lot numbers and product codes.
Stryker recalls specific Synchro2 guidewires with hydrophilic coating that may have manufacturing defects. Affected units include certain lot numbers and product codes. Consumers should check their product details and contact Stryker for instructions.
Stryker recalls Synchro2 guidewires with incorrect outer diameter label (0.036mm instead of 0.36mm). This could lead to improper use in medical procedures. Affected units include specific lot numbers and product codes.
Stryker recalls Synchro2 guidewires with incorrect outer diameter label (0.036mm instead of 0.36mm). This may lead to improper use during medical procedures. Affected units include specific lot numbers and product codes.
Stryker recalls Synchro2 guidewires with incorrect outer diameter labeling (0.036mm instead of 0.014in). This could lead to improper use in medical procedures. Affected units include specific product numbers and lot numbers.
Stryker recalls Synchro2 0.014in x 200cm STANDARD Guidewire with Hydrophilic Coating due to incorrect millimeter label (0.036mm listed instead of 0.36mm). This could lead to improper use during medical procedures. Affected units include specific lot numbers.
Stryker recalls Synchro2 guidewires with incorrect outer diameter label (0.036mm instead of 0.014in). This could lead to improper use in medical procedures. Affected units include specific lot numbers.
Stryker recalls Synchro2 guidewires with incorrect outer diameter label (0.036mm instead of 0.36mm). This could lead to improper use during medical procedures. Affected units include specific lot numbers and product codes.
Stryker is recalling Wingspan Stent System (Rx Only, Sterile EO) due to reported use-related coating damage on delivery catheter shafts. Affected units have specific catalog numbers. No remedy is stated in the recall notice.
Stryker recalls specific AXS Infinity LS Long Sheath models due to outer diameter specification being exceeded. Affected units include GEN-10800-70, GEN-10800-80, and GEN-10800-90 models. No remedy is stated in the recall notice.
Stryker recalls FlowGate2 Balloon Guide Catheters with specific sizes due to potential balloon size issues that may prolong procedures during medical use.
Stryker Neurovascular recalls Trevo XP ProVue System kits with mismatched carton sleeve and contents. Affected kits may have incorrect packaging. No immediate action needed as the hazard is cosmetic.
Stryker recalls certain stroke intervention kits due to potential mismatch between carton labels and actual contents. Affected kits may contain incorrect components, risking improper use during medical procedures.
Stryker recalls some Stroke Fast Packs and Trevo Procedure Packs due to mismatched carton labels and actual contents. Affected units may have incorrect items inside the packaging.
Stryker recalls some Stroke Fast Packs and Trevo Procedure Packs due to mismatched carton labels and actual contents. Affected units may have incorrect contents, but no injury reports. Consumers should check labels and contact Stryker for details.
