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ARROW IPN925140Recalls & reported problems

Teleflex Incorporated · Arrowg+ard Blue(R) MAC(TM) Two-Lumen Central Venous Access for use with 7.5 - 8 Fr. Catheters · 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 10801902210996), received between Oct 29, 2025 and Oct 29, 2025 — classified as 1 malfunction.

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

10 other recalls cover devices cleared under the same FDA submission (K940079); 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: 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: 1 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 Discolored1

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.

  • MalfunctionOct 29, 2025Material Discolored

    PRIOR TO INSERTION OF CENTRAL LINE DILATOR THAT THE TIP LOOKED DIFFERENT WITH A DRIED RUST COLOR.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23411935 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K940079. One submission often covers many models, so check the product and lot details in each record.

  • Z-2385-2026 · Apr 21, 2026 · Open, Classified
    Description/REF: ACCESS TRAY/GU-04020; PSI KIT: 8.5 FR/AK-09803-CDC; PSI KIT: 9 FR/AK-09903-CDC; PSI KIT: 8.5 FR X 4 IN (10 CM)/ASK-09810-PCMH1; PSI KIT: 9 FR X 10 CM/ASK-09903-KH;
  • Z-1986-2018 · Apr 11, 2018 · Terminated
    Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R) Sheath, Integral Hemostasis Valve/Side Port, Sharps Safety Features, and Maximal Barrier Precautions for use with 7.5 - 8
  • Z-1975-2018 · Apr 11, 2018 · Terminated
    Arrow-Flex(R) Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R) Sheath and Integral Hemostasis Valve/Side Port for use with 7.5 - 8 Fr. Catheters ; Product Codes: ASK-0990
  • Z-2017-2018 · Apr 11, 2018 · Terminated
    Percutaneous Sheath Introducer Kit with ARROWgard Blue Sheath and Integral Hemostasis Valve/Side Port for use with 7 - 7.5 Fr. Catheters; Product Codes: MSO-29802-AHS and MSO-29903
  • Z-2018-2018 · Apr 11, 2018 · Terminated
    ARROWgard Blue PLUS Multi-Lumen CVC Kit with Blue FlexTip Catheter; Product Code: MSO-45703-AHS
  • Z-1334-2018 · Dec 22, 2017 · Terminated
    Arrowg+ard Blue(R) PSI Kit, (1) For use with 7 - 7.5 Fr. Catheters Part Number (PN): ASK-29804-UHN2; (2) For use with 7.5 - 8 Fr. Catheters PN: ASK-29903-UCD
  • Z-1160-2018 · Nov 14, 2017 · Terminated
    Percutaneous Sheath Introducer Kit with ARROWg+ard Blue Sheath, Integral Hemostasis Valve/Side Port, Sharps Safety Features, and Maximal Barrier Precautions for use with 7.5 - 8 Fr
  • Z-0784-2010 · Nov 24, 2009 · Terminated
    Percutaneous Sheath Introducer Kit with ARROWg+ard Blue (R) Sheath, Integral Hemostasis Valve/Side Port, Sharps Safety Features and Maximal Barrier Precautions for use with 7.5 - 8
  • Z-1492-2009 · Feb 11, 2009 · Terminated
    Arrow ARROWg+ard Super Arrow-Flex Percutaneous Sheath Introducers
  • Z-1035-03 · Jul 8, 2003 · Terminated
    9 French Super Arrow-Flex Percutaneous Sheath Introducer Kit with Arrowg and Blue Antimicrobial Surface Sheath

Other Introducer, catheter devices

All Introducer, catheter devices →

Sources and updates

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