AXS VECTA 71 INC-11129-125Recalls & reported problems
Stryker Corporation · Intermediate Catheter · Class 2
All models of AXS VECTA 71 (3)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327459227), received between Mar 28, 2023 and Dec 17, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fracture” (1 report).
1 other recall cover devices cleared under the same FDA submission (K172167, K190212, K190833, K191768, K200206); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture1
- Peeled/Delaminated1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 17, 2025Peeled/Delaminated; Peeled/Delaminated
IT WAS REPORTED THAT DURING THE PROCEDURE THE DISTAL MARKERS OF SUBJECT CATHETER GOT STUCK ON THE LIP OF BASE CATHETER AND THE INNER LINING OF THE SUBJECT CATHETER CAME OFF. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO CLINICAL CONSEQUENCES WERE REPORTED TO THE PATIENT DUE TO THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23830515 ↗MalfunctionMar 28, 2023Fracture; Fracture
IT WAS REPORTED THAT THE CATHETER (SUBJECT DEVICE) STRIPPED AND PULLED APART WHILE REMOVING FROM PATIENT. ALL PARTS WERE CONTAINED AND REMOVED SAFELY FROM PATIENT. NO CLINICAL CONSEQUENCES WERE REPORTED TO THE PATIENT DUE TO THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16632253 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K172167, K190212, K190833, K191768, K200206. One submission often covers many models, so check the product and lot details in each record.
- Z-1620-2020 · Apr 10, 2019 · TerminatedStryker Neurovascular, AXS Vecta 71 Aspiration Catheter, Ref. Catalog No. INC-11129-115, Use By 2021-11-29, Rx Only, Sterile/EO, Manufactured For: Stryker Neurovascular 47900 Baysi
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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