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ARROW IPN923902Recalls & reported problems

Teleflex Incorporated · Percutaneous Sheath Introducer Set with Integral Hemostasis Valve/Side Port for use with 7 Fr. Catheters · Class 2

Data updated Oct 13, 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 10801902207002), received between Apr 8, 2026 and Apr 8, 2026 — classified as 1 malfunction.

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

17 other recalls cover devices cleared under the same FDA submission (K780532); 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.

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: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 1 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

  • Break1

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.

  • MalfunctionApr 8, 2026Break

    IT WAS REPORTED THAT: "WHEN INSERTING THE CATHETER, THE GUIDE BREAKS WITHOUT APPLYING EXCESSIVE FORCE.THERE WAS NO REPORTED PATIENT HARM.".

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24813809 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K780532. 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-1242-2020 · Dec 20, 2019 · Terminated
    Arrow PSI Kit for use with 7 - 7.5 Fr. Catheters ASK-09801-UPM
  • Z-2576-2018 · May 23, 2018 · Terminated
    Percutaneous Sheath Introducer Kit for use with 7 - 7.5 Fr. Catheters (8 Fr. 10 cm sheath length .035 inch dia. spring-wire guide), REF ES-09807. The percutaneous sheath introduc
  • Z-2011-2018 · Apr 11, 2018 · Terminated
    Spring-Wire Guide Introducer Catheter Assembly; Product Code: CN-04018
  • Z-2032-2018 · Apr 11, 2018 · Terminated
    9 Fr. Radiopaque Polyurethane Sheath/Dilator with Integral Hemostasis Valve/Side Port for use with 7 - 8 Fr. Catheters and Arrow Percutaneous Introducer System; Product codes: SS-0
  • Z-1976-2018 · Apr 11, 2018 · Terminated
    Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port for use with 7.5 - 8 Fr. Catheters; Product Code: ASK-09903-UPA
  • Z-1977-2018 · Apr 11, 2018 · Terminated
    Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port and Sharps Safety Features (Recommended for use with 7 Fr. Catheters); Product Code: ASK-09907-SB
  • Z-2031-2018 · Apr 11, 2018 · Terminated
    ARROWg+ard Blue PSI Kit with Integral Hemostasis Valve/ Side Port for use with 7 - 7.5 Fr. Catheters; Product codes: SF-29803-1
  • Z-1329-2018 · Dec 22, 2017 · Terminated
    (1) Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port, Sharps Safety Features, and Maximal Barrier Precautions for use with 7.5 - 8 Fr. Catheters, Part Nu
  • Z-1158-2018 · Nov 14, 2017 · Terminated
    Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port, Sharps Safety Features and Maximal Barrier Precautions for use with 7.5 - 8 Fr. Catheters. Permits ven
  • Z-1287-2018 · Oct 26, 2017 · Terminated
    Arterial Access Tray, introducer catheter; Model: GU-04020
  • Z-2329-2017 · May 9, 2017 · Terminated
    1) Introducer Kit with Integral Hemostasis Valve/Side Port, Sharps Safety Features, and Maximal Barrier Precautions for use with 7.5 - 8 Fr., Introducer Catheter 2) Arrow PSI Kit
  • Z-0066-2015 · Aug 6, 2014 · Terminated
    Arrow Select Kits (ASK) and Maximal Barrier Precautions Kits (CDC) with BD Medical Posiflush 10mL Saline Flush Syringe.
  • Z-1713-2014 · Apr 14, 2014 · Terminated
    Arrow Percutaneous Sheath Introducer Kits The Percutaneous sheath introducer products permit venous or arterial access and device introduction to the central circulation.
  • Z-0468-2014 · Oct 9, 2013 · Terminated
    Arrow Transradial Artery Access products Arrow Transradial Artery Access products are used for percutaneous introduction of devices into the radial artery for diagnostic and thera

…and 2 more.

Other Introducer, catheter devices

All Introducer, catheter devices →

Sources and updates

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