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ARROW IPN038325Recalls & reported problems

Teleflex Incorporated · Two-Lumen Hemodialysis Catheterization Set with Blue FlexTip(R) ARROWg+ard Blue(R) Catheter for High Volume Infusions · Class 2

All models of ARROW (1494)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10801902139259), received between Nov 11, 2021 and Nov 11, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Unraveled Material” (1 report).

5 other recalls cover devices cleared under the same FDA submission (K993933); 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 16, 2026.

Most reported problems

Device problems

  • Unraveled Material1

Patient problems

  • Pain1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionNov 11, 2021Unraveled Material; Unraveled Material

    IT WAS REPORTED THAT: INCIDENT HAPPENED DURING THE INSERTION OF A DIALYSIS CATHETER. THE INCIDENT HAPPENED AT THE TIME OF REMOVING THE GUIDE. THE GUIDE GOT STUCK IN THE DILATOR AND "FELL APART". SO THE DOCTOR DECIDED TO REMOVE THE DEVICE. NO PATIENT HARM REPORTED. IT WAS REPORTED THE DEVICE WAS REMOVED AND ANOTHER DEVICE INSERTED, "SO IT WAS PAINFUL FOR THE PATIENT".

    Patient problems: Pain

    MAUDE report 12800799 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K993933. One submission often covers many models, so check the product and lot details in each record.

  • Z-2373-2026 · Apr 21, 2026 · Open, Classified
    Description/REF: HEMODIALYSIS KIT: 2-LUMEN 8 FR X 11 CM/AK-11802-F; HEMODIALYSIS KIT: 2-LUMEN 12 FR X 16 CM/AK-22122; HEMODIALYSIS KIT 2L: 14 FR X 15CM AGB/AK-22142-CDC; HEMODIALYS
  • Z-1336-2018 · Dec 22, 2017 · Terminated
    ARROWg+ard Blue Two-Lumen Hemodialysis Catheterization Kit for High Volume Infusions (1) Part Number (PN): CDC-22122-1A; (2) PN: CDC-25122-1A; (3) PN: CDC-25142-1A; (4) CDC-26142-1
  • Z-0658-2018 · Oct 17, 2017 · Terminated
    ARROWg+ard Blue Two Lumen Hemodialysis Catheterization Kit for High Volume Infusions; Product Codes: AK-22142-CDC, AK-22142-F, AK-25142-CDC, AK-25142-F; Exp. Dates Feb 2018 - Nov 2
  • Z-2334-2017 · May 9, 2017 · Terminated
    1) ARROWg+ard Blue You-Blend Two-Lumen Hemodialysis Catheterization Kit for High Volume Infusions The large-bore two-lumen catheter permits venous access to the central circulation
  • Z-0639-04 · Feb 18, 2004 · Terminated
    Two Lumen 14F Hemodialysis Catheter Kits/Sets with Blue FlexTip Arrowg+ard Blue Curved Catheter for high Volume Ifusions

Other CATHETER, HEMODIALYSIS, NON-IMPLANTED devices

All CATHETER, HEMODIALYSIS, NON-IMPLANTED devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page