Stryker Neurovascular recalls
Every recall we track for Stryker Neurovascular — 39 in all, from 2017–2026 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from Stryker Neurovascular dropped to zero in 2025 (0, down from 13 in 2024). 3% rated “stop using now”.
All FDA recall records for Stryker Neurovascular since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 8 | 0 | 8 |
| 2018 | 0 | 1 | 8 | 3 | 12 |
| 2019 | 0 | 3 | 0 | 0 | 3 |
| 2020 | 0 | 1 | 0 | 0 | 1 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 1 | 0 | 1 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 1 | 3 | 8 | 1 | 13 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 1 | 0 | 0 | 1 |
What to do if you have a recalled Stryker Neurovascular product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Stryker Neurovascular recalls
17 shown- Use cautionMedical device
Stryker Neurovascular recalls INZONE DETACHMENT SYSTEM, REF: M00345100950
Stryker recalls INZONE Detachment System devices with premature battery drain causing failure to power on or detach coils, potentially requiring medical intervention.
StrykerApr 6, 2026 - Lower riskMedical device
Stryker Neurovascular recalls The Trevo Trak 21 Microcatheter is a single-lumen, braided shaft, variable stiffness catheter with radiopaque marker(s)
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 NeurovascularAug 30, 2024 - UnratedMedical device
Stryker Neurovascular recalls Trevo ProVue, Catalog: 90184
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.
StrykerApr 23, 2024 - Use cautionMedical device
Stryker Neurovascular recalls The Synchro2 Guidewires are a steerable guidewire family with a shapeable tip and are available in straight and
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 NeurovascularApr 18, 2024 - Lower riskMedical device
Stryker Neurovascular recalls The Distal Access Catheter is a single-lumen, braided shaft, variable stiffness catheter with radiopaque marker on the
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 NeurovascularApr 3, 2024 - Lower riskMedical device
Stryker Neurovascular recalls Trevo Trak 21 Microcatheter, REF: 90338. TREVO NXT 3X32+TRAK21 2-PACK - CE, REF: 91412; TREVO NXT 4X28+TRAK21 2-PACK -
Stryker recalls specific Trevo Trak 21 Microcatheter models due to missing product drawing on carton labels. This may affect medical device safety during procedures.
StrykerJun 3, 2022 - Use cautionMedical device
Stryker Neurovascular recalls Trevo XP ProVue Retriever, REF (Size): 90182 (4MM x 20MM); 90185 (4MM x 30MM); 90186 (6MM x 25MM). Procedure Pack REF:
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.
StrykerSep 21, 2020 - Use cautionMedical device
Stryker Neurovascular recalls Stryker Neurovascular, AXS Infinity LS Plus Long Sheath, Rx Only, Sterile EO, USA Customer Service 855-91 NEURO
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 NeurovascularApr 18, 2019 - Use cautionMedical device
Stryker Neurovascular recalls Stryker Neurovascular, AXS Vecta 71 Aspiration Catheter, Ref. Catalog No. INC-11129-115, Use By 2021-11-29, Rx Only,
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 NeurovascularApr 10, 2019 - Lower riskMedical device
Stryker Neurovascular recalls Stryker Neurovascular, Merci 9F, 80cm, Balloon Guide Catheter, REF 90077, CE 0459, UPN Product No. 90077, UDI #:
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 NeurovascularNov 13, 2018 - Lower riskMedical device
Stryker Neurovascular recalls Synchro2, 0.014 in x 200cm, SOFT Guidewire with Hydrophilic Coating, UPN Product No. M00326010 REF 2601, STERILE: EO -
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.
StrykerJun 8, 2018 - UnratedMedical device
Stryker Neurovascular recalls Wingspan Stent System, Rx Only, Sterile EO, Catalog #: M003WE0250090, M003WE0300090, M003WE0350090, M003WE0400090,
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 NeurovascularJun 5, 2018 - UnratedMedical device
Stryker Neurovascular recalls AXS Infinity LS Long Sheath:((6F/.088in)/ x 70cm GEN-10800-70, (6F/.088in)/ x 80cm GEN-10800-80, (6F/.088in)/ x 90cm
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.
StrykerMay 2, 2018 - Use cautionMedical device
Stryker Neurovascular recalls FlowGate2 Balloon Guide Catheter, UPN 90485 (8Fx85cm size) and 90495 (8Fx95cm size)
Stryker recalls FlowGate2 Balloon Guide Catheters with specific sizes due to potential balloon size issues that may prolong procedures during medical use.
StrykerApr 11, 2018 - Lower riskMedical device
Stryker Neurovascular recalls Trevo XP ProVue System kit containing 1) Trevo XP ProVue Retriever, 4x20mm and 2) Trevo Pro18 Microcatheter
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 NeurovascularNov 28, 2017 - Lower riskMedical device
Stryker Neurovascular recalls Stroke Fast Pack(TM), Trevo(TM) XP, TREVO(TM) XP PROVUE RETRIEVER, 4 mm, 20 mm, ; Trevo(TM) Pro 18, TREVO PRO 18
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.
StrykerNov 3, 2017 - Lower riskMedical device
Stryker Neurovascular recalls Stroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 20, Trevo Pro 18 Microcatheter, AXS Catalyst 060x132CM - US, UPN
Stryker Neurovascular recalls some Stroke Fast Packs due to mismatched carton sleeve labels and physical contents. Affected units include specific lot numbers and model codes. Consumers should check their packaging for the listed identifiers.
Stryker NeurovascularJun 26, 2017
Stryker Neurovascular recall questions
How many recalls has Stryker Neurovascular had?
39 recalls from Stryker Neurovascular are on record with U.S. safety agencies, from 2017–2026.
What is the most recent Stryker Neurovascular recall?
Stryker Neurovascular recalls INZONE DETACHMENT SYSTEM, REF: M00345100950, dated Apr 6, 2026. Every Stryker Neurovascular recall is listed on this page, newest first.
What should I do if I have a recalled Stryker Neurovascular product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Stryker Neurovascular recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.