Skip to content

ARROW IPN036476Recalls & reported problems

Teleflex Incorporated · Pressure Injectable Multi-Lumen Central Venous Catheterization Kit · 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
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 60801902124342), received between Jan 17, 2024 and Jan 17, 2024 — classified as 1 injury.

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

54 other recalls cover devices cleared under the same FDA submission (K071538); 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: 1 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 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

  • Material Separation1

Patient problems

  • Cough1
  • Foreign Body In Patient1

Recent adverse event reports

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

  • InjuryJan 17, 2024Material Separation; Material Separation

    IT WAS REPORTED THAT: "UPON REMOVAL OF THE CATHETER, IT WAS NOTED THAT THE TIP WAS MISSING. IMAGING CONFIRMED THAT THE TIP WAS STILL IN THE PATIENT. ATTEMPTS TO REMOVE THE CATHETER TIP/FRAGMENT WERE UNSUCCESSFUL. THERE WERE NO COMPLICATIONS DURING LINE PLACEMENT. REMOVAL OF THE LINE WENT WELL AND WAS WITHOUT DIFFICULTY". ADDITIONAL INFORMATION: PATIENT WAS BROUGHT TO THE CATH LAB TO ATTEMPT TO REMOVE THE TIP BUT THEY WERE UNSUCCESSFUL. THE PATIENT WAS DISCHARGED HOME WITH THE TIP STILL IN THE VESSEL. THE PATIENT INFORMED THE MD ABOUT A PERSISTENT COUGH SOMETIME LATER. THEY ARE DUE TO SEE A RESPIRATORY SPECIALIST TO DETERMINE WHETHER THE FRAGMENT NEEDS TO BE REMOVED. AWAITING ADDITIONAL INFORMATION.

    Patient problems: Cough; Foreign Body In Patient

    MAUDE report 18526588 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K071538. One submission often covers many models, so check the product and lot details in each record.

  • Z-2376-2026 · Apr 21, 2026 · Open, Classified
    Description/REF: CVC/PSI KIT: 2 LUMEN 8 FR X 6 IN/ASK-42802-PLH; CVC KIT: 3-LUMEN 12 FR X 16 CM/AK-12123-F; CVC KIT: 3-LUMEN 12 FR X 20 CM/AK-15123-F; 3L CVC KIT: 7 FR X 16 CM/ASK-
  • Z-1914-2026 · Mar 11, 2026 · Open, Classified
    ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS CATHETER REF ASK-42802-PLH UDI code: (01)10801902133110(17)261231(11)251211(10)33F25L0140 REF ASK-4
  • Z-2123-2026 · Jan 7, 2026 · Open, Classified
    Medline Convenience Kits: 1) KIT TRIPLE LUMEN INSERTION, Model Number: DYNDM1031A
  • Z-0003-2024 · Aug 10, 2023 · Open, Classified
    Arrow Pressure Injectable Arrowg+ard Blue Plus Four-Lumen CVC, REF CDC-45854-P1A; catheter, intravascular, therapeutic, long-term greater than 30 days
  • Z-0002-2024 · Aug 10, 2023 · Open, Classified
    Arrow ErgoPack Complete, Pressure Injectable Arrowg+ard Blue Plus Four-Lumen CVC, REF CDC-42854- PCN1A; catheter, intravascular, therapeutic, long-term greater than 30 days
  • Z-0352-2023 · Oct 27, 2022 · Terminated
    Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit, REF numbers: a) ASK-42703-NS, b) ASK-42703-PCCH2, c) ASK-42703-PUPM1, d) ASK-45703-NS, e) ASK-45703-PAU, f) ASK-45703-
  • Z-0351-2023 · Oct 27, 2022 · Terminated
    Arrow MAC Two-Lumen Central Venous Access Kit fr use with 7 - 7.5 Fr Catheters, REF ASK-11242-UPM1; catheter introducer
  • Z-1604-2022 · May 25, 2022 · Open, Classified
    TELEFLEX LLC Arrow Central Venous Catheter Kit 16, 18 Gauge Multi Lumen Model Number:CDC-45703-XP1A (Model Numbers # IPN035619, IPN036437, IPN922677)
  • Z-1989-2018 · Apr 11, 2018 · Terminated
    ARROWg+ard Blue PLUS Pressure Injectable Quad-Lumen CVC Kit; Product Codes: CDC-42854-P1A and CDC-45854-P1A
  • Z-1991-2018 · Apr 11, 2018 · Terminated
    Pressure Injectable Quad-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features; Product Codes: ASK-45854-PSFM a
  • Z-1992-2018 · Apr 11, 2018 · Terminated
    ARROWg+ard Blue PLUS Pressure Injectable Two-Lumen CVC Kit; Product Code: CDC-42802-P1A
  • Z-1994-2018 · Apr 11, 2018 · Terminated
    ARROWg+ard Blue PLUS Pressure Injectable Multi-Lumen CVC Kit; Product Codes: CDC-45703-P1A; CDC-45703-PB1A; CDC-42703-P1A; and CDC-15703-P1A
  • Z-1998-2018 · Apr 11, 2018 · Terminated
    Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter, Sharps Safety Features and Maximal Barrier Precautions; Product Code: ASK-427
  • Z-1995-2018 · Apr 11, 2018 · Terminated
    Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip, ARROWg+ard Blue PLUS Catheter, Sharps Safety Features and Maximal Barrier Precautions; Product
  • Z-2000-2018 · Apr 11, 2018 · Terminated
    ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous Catheterization Kit; Product Code: ASK-42703-SJH

…and 39 more.

Other Catheter, intravascular, therapeutic, short-term less than 30 days devices

All Catheter, intravascular, therapeutic, short-term less than 30 days devices →

Sources and updates

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