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ARROW IPN921102Recalls & reported problems

Teleflex Incorporated · Percutaneous Sheath Introducer Set with Integral Hemostasis Valve/Side Port for use with 7.5 Fr. Catheters · Class 2

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 10801902200102), received between Apr 24, 2026 and Apr 24, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Separation” (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

  • Material Separation1

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 24, 2026Material Separation

    IT WAS REPORTED THAT: AT INSERTION OF THE SHEATH, THE CONNECTION BETWEEN THE GUARD AND THE SHEATH BODY GOT DETACHED AND THE SHEATH BODY DETACHED FROM THE GUARD. CHECKING IT, THE CONNECTING PART WAS LOOSENED, SO A NEW KIT WAS USED TO COMPLETE THE PROCEDURE. NO INJURY TO THE PATIENT OCCURRED."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24976701 ↗

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-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-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-2011-2018 · Apr 11, 2018 · Terminated
    Spring-Wire Guide Introducer Catheter Assembly; Product Code: CN-04018
  • 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-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-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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.