ARROW IPN914738Recalls & reported problems
Teleflex Incorporated · Two-Lumen CVC · Implant
All models of ARROW (1494)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10801902157703), received between Aug 17, 2021 and Aug 17, 2021 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Deformation Due to Compressive Stress” (3 reports).
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.
Most reported problems
Device problems
- Deformation Due to Compressive Stress3
Patient problems
- Insufficient Information2
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 17, 2021Deformation Due to Compressive Stress; Deformation Due to Compressive Stress
IT WAS REPORTED "THE GUIDE WIRE BENT AND COULD NOT BE PULLED OUT" DURING THE INSERTION PROCESS. THE ATTEMPT TO REMOVE THE WIRE OUT OF THE CATHETER FAILED AS THE SPRING WIRE GUIDE WAS KINKED. A NEW DEVICE WAS USED WITHOUT ANY ISSUE. NO PATIENT HARM REPORTED. THE PATIENT'S CONDITION IS REPORTED AS FINE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12333601 ↗MalfunctionAug 17, 2021Deformation Due to Compressive Stress; Deformation Due to Compressive Stress
IT WAS REPORTED "THE GUIDE WIRE BENT AND COULD NOT BE PULLED OUT." NO PATIENT HARM WAS REPORTED.
Patient problems: Insufficient Information
MAUDE report 12333561 ↗MalfunctionAug 17, 2021Deformation Due to Compressive Stress; Deformation Due to Compressive Stress
IT WAS REPORTED "THE GUIDE WIRE BENT AND COULD NOT BE PULLED OUT". NO PATIENT HARM WAS REPORTED.
Patient problems: Insufficient Information
MAUDE report 12333538 ↗
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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