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ARROW IPN033624Recalls & reported problems

Teleflex Incorporated · Three-Lumen CVC for use only with Arrow Percutaneous Sheath Introducer (8.5 Fr. and 9 Fr.) · Class 2 · Implant

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 00801902100368), received between Aug 26, 2024 and Aug 26, 2024 — classified as 1 malfunction.

The most frequently reported specific device problem is “Gas/Air Leak” (1 report).

24 other recalls cover devices cleared under the same FDA submission (K862056); 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.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 1 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Gas/Air Leak1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionAug 26, 2024Gas/Air Leak; Gas/Air Leak

    IT WAS REPORTED THAT: "PATIENT WAS ADMITTED TO THE SICU FROM THE OPERATING ROOM, UPON ADMISSION RN WAS CHECKING PATIENT'S CENTRAL LINE. THE INTRODUCER HAD A TRIC CATHETER IN PLACE, WHEN ATTEMPTED TO DRAW BACK BLOOD ABOUT 10 MLS OF AIR WAS RETURNED. BECAUSE OF THIS FLUSHING THE LINE WAS NOT ATTEMPTED. THIS WAS TRUE FOR ALL THREE PORTS OF THE TRIC CATHETER. THE SIDEARMS OF THE INTRODUCER DREW BACK BLOOD AND FLUSHED WITHOUT ISSUE. THE ICU TEAM WAS AWARE AND THE TRIC WAS REMOVED. UPON INSPECTION OF THE CATHETER AFTER REMOVAL THERE DID NOT APPEAR ANY OBVIOUS DEFECT. CATHETER WAS SAVED FOR INSPECTION." THERE WAS NO REPORTED PATIENT HARM.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 20062812 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K862056. One submission often covers many models, so check the product and lot details in each record.

  • Z-2377-2026 · Apr 21, 2026 · Open, Classified
    Description/REF: ARTERIAL LINE KIT: SL 20 GA X 5 IN/ASK-04510-MM6 RA CATH KIT: 20 GA X 1-3/4IN/NA-04020-X1ASP ACCESS TRAY/ASK-04001-MS RA CATH KIT: 20 GA X 8 CM/ASK-00820-UM1 VESSE
  • Z-1118-2019 · Jan 10, 2019 · Terminated
    Arrow Two-Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter Product Code: AH-11802 (OUS) GTN: 00801902026132
  • Z-1119-2019 · Jan 10, 2019 · Terminated
    Arrow Two-Lumen Central Venous Catheterization Set with Blue FlexTip Catheter Product Code: CD-10802 GTN: 00801902015396
  • Z-0723-2019 · Nov 14, 2018 · Terminated
    Arrow CVC 2 Lumen, Pediatric Two-Lumen Central Venous Cauterization Set with Blue FlexTip Catheter, 4 Fr 2 Lumen 5cm, Reference # CS-12402 The Arrow CVC is intended to provide sho
  • Z-2818-2018 · Jul 10, 2018 · Terminated
    HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use only with Arrow One-Piece Percutaneous Sheath Introducer System, Material HO-14702 The central venous cathe
  • Z-2819-2018 · Jul 10, 2018 · Terminated
    HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use only with Arrow One-Piece Percutaneous Sheath Introducer System, Material HO-14703 The central venous cath
  • Z-2336-2018 · May 11, 2018 · Terminated
    Multi-Lumen Central Venous Catheterization Set with Blue FlexTip Catheter, CS-15853-E Product CVCs are intended to permit venous access to the central circulation through a single
  • Z-1967-2018 · Apr 11, 2018 · Terminated
    Maximal Barrier Drape; Product Code: ASK-04000-HMC
  • Z-1978-2018 · Apr 11, 2018 · Terminated
    Two-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter and Sharps Safety Features; Product Code: ASK-15402-HOP
  • Z-1982-2018 · Apr 11, 2018 · Terminated
    ARROWg+ard Blue(R) MAC(TM) Two-Lumen Central Venous Access Kit for use with 7-7.5 Fr. Catheters; Product Code: ASK-21142-WHC2
  • Z-1332-2018 · Dec 22, 2017 · Terminated
    (1) Access Tray, Part Number (PN): ASK-04001-MS; Arrow Multi-Lumen CVC Kit (2) PN: CDC-12703-1A; (3) PN: CDC-15703-1A; (4) PN: CDC-15703-B1A; Arrow Two-Lumen CVC Kit (5) PN: CDC-12
  • Z-0648-2018 · Oct 17, 2017 · Terminated
    Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter and Sharps Safety Features; Product Code: ASK 15703 NYP; Exp. Dates Feb 2018 - Nov 2018
  • Z-0650-2018 · Oct 17, 2017 · Terminated
    Multi Lumen Central Venous Catheterization Kit; Product Code: ASK-12703-HH2; Exp. Dates Feb 2018 - Nov 2018
  • Z-0654-2018 · Oct 17, 2017 · Terminated
    Arrow Multi Lumen CVC Kit (Central venous catheter); Product Code: CDC-15703-1A; Exp. Dates Feb 2018 - Nov 2018
  • Z-0652-2018 · Oct 17, 2017 · Terminated
    Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter, Sharps Safety Features, and Maximal Barrier Precautions Features; Product Code: ASK-12703-WMC1; Exp. Dat

…and 9 more.

Other CATHETER, PERCUTANEOUS devices

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Sources and updates

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