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, ClassifiedDescription/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 · TerminatedARROWg+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 · TerminatedARROWg+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 · Terminated1) 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 · TerminatedTwo Lumen 14F Hemodialysis Catheter Kits/Sets with Blue FlexTip Arrowg+ard Blue Curved Catheter for high Volume Ifusions
Other CATHETER, HEMODIALYSIS, NON-IMPLANTED devices
- MAHURKAR 8888135191Mozarc Medical US LLC · CATHETER, HEMODIALYSIS, NON-IMPLANTED1 recall175 reports
- MAHURKAR 8888135241Mozarc Medical US LLC · CATHETER, HEMODIALYSIS, NON-IMPLANTED1 recall1 death100 reports
- ARROW IPN036723Teleflex Incorporated · CATHETER, HEMODIALYSIS, NON-IMPLANTED2 recalls2 reports
- DuoGlide catheter 5625240Bard Access Systems, Inc. · CATHETER, HEMODIALYSIS, NON-IMPLANTED2 recalls1 report
- ARROW IPN036412Teleflex Incorporated · CATHETER, HEMODIALYSIS, NON-IMPLANTED2 recalls1 report
- ARROW IPN036419Teleflex Incorporated · CATHETER, HEMODIALYSIS, NON-IMPLANTED2 recalls0 reports
- ARROW IPN927343Teleflex Incorporated · Catheter, hemodialysis, non-implanted2 recalls0 reports
- ARROW IPN036428Teleflex Incorporated · CATHETER, HEMODIALYSIS, NON-IMPLANTED2 recalls0 reports
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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