ARROW IPN927345Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10801902213539), received between Jul 8, 2024 and Jun 9, 2025 — classified as 2 malfunctions.

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

1 FDA recall record name this device's identifier, 1 still open.

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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

1. Apr 21, 2026Open, Classified

   Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.

   Z-2388-2026 · Root cause: Nonconforming Material/Component · FDA record ↗

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 9, 2025Material Deformation; Material Deformation

  IT WAS REPORTED "INSERTER OBSERVED A DEFECT IN THE J-TIP OF THE WIRE PRIOR TO USE." THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22167616 ↗
• MalfunctionJul 8, 2024Break; Material Separation; Break; Material Separation

  IT WAS REPORTED THAT: "WIRE BROKE DURING DIALYSIS CATHETER PLACEMENT RESULTING IN THE PATIENT REQUIRING A SECOND PROCEDURE. PROCEDURE NOTE: 1ST ATTEMPT COMPLICATED BY SHEARING AND SEPARATION OF OVERLYING GUIDEWIRE SPRINGS AT CATHETER MID-POINT. BOTH PIECES OF THE WIRE WERE RETRIEVED FROM THE PATIENT SUCCESSFULLY. 2ND ATTEMPT USED COMPLETELY NEW LINE KIT AND LINE PLACED WITHOUT DIFFICULTY. PATIENT NOTIFIED OF PROCEDURAL/EQUIPMENT COMPLICATION IMMEDIATELY AFTERWARDS. POST-PROCEDURE CXR CONFIRMED NO RETAINED WIRE PRODUCTS." THE PATIENT WAS REPORTED AS FINE.

  Patient problems: Foreign Body In Patient

  MAUDE report 19687366 ↗

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