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ARROW IPN037098Recalls & reported problems

Teleflex Incorporated · QuickFlash(R) Radial Artery Catheterization Kit · Class 2

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20801902121619), received between Oct 20, 2021 and Oct 20, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Damaged by Another Device” (1 report).

1 FDA recall record name this device's identifier, 1 still open.

32 other recalls cover devices cleared under the same FDA submission (K810675); 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.

Recalls naming this device

  1. Feb 12, 2024Open, Classified

    Teleflex is initiating this voluntary recall for the above-mentioned products due to reports received indicating a potentially defective component. The complaints received relate to resistance of the guidewire handle/chamber during use. The possible immediate health consequences of the component issue are arterial vasospasm and vessel injury arising from multiple arterial punctures with repeated attempts.

    Z-1267-2024 · Root cause: Process control · FDA record ↗

Most reported problems

Device problems

  • Device Damaged by Another Device1

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 20, 2021Device Damaged by Another Device; Device Damaged by Another Device

    THE NEEDLE PIERCED THE CATHETER DURING INSERTION. NO PATIENT HARM REPORTED. IT WAS REPORTED THE PATIENT'S CONDITION WAS BELIEVED TO NOT BE CRITICAL AND NO INTERVENTION WAS REQUIRED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12668430 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K810675. One submission often covers many models, so check the product and lot details in each record.

  • Z-2397-2026 · Apr 21, 2026 · Open, Classified
    Description/REF: RA CATH KIT: 20 GA X 1-1/2IN/NA-04220-1A; RA CATH KIT: 20 GA X 1-1/2IN/NA-04220-X1A; ARTERIAL CATHETER KIT: 18 GA X 16 CM/ASK-04018-HCA; ARTERIAL CATHETER KIT: 18
  • Z-3299-2024 · Jul 26, 2024 · Open, Classified
    Arrow Arterial Kits and Trays as follows: (1) Arrow Arterial Access Tray with 0.025" Spring-Wire Guide (Catheter Not Included), REF ASK-04001-BW1; (2) Arrow Arterial Access Tray
  • Z-0844-2020 · Dec 12, 2019 · Open, Classified
    Arrow Arterial Catherization Kit-20 Ga. x 4.45 cm Radiopaque Polyurethane over 22 Ga. TW Introducer Needle with Integral .018" (0.46 mm) dia. Spring-Wire Guide Product Code: ASK-04
  • Z-1970-2018 · Apr 11, 2018 · Terminated
    Radial Artery Catheterization Kit; Product Codes: ASK-04020-AH, ASK-04020-MIHS, ASK-04120-HF1
  • Z-1971-2018 · Apr 11, 2018 · Terminated
    Arterial Catheterization Kit; Product Codes: ASK-04020-DH
  • Z-1968-2018 · Apr 11, 2018 · Terminated
    Radial Arterial Access Kit; Product Code: ASK-04001-BID2
  • Z-2019-2018 · Apr 11, 2018 · Terminated
    Arterial Catheterization Kit; Product Code:NA-04550-1A
  • Z-1969-2018 · Apr 11, 2018 · Terminated
    Arterial Line Kit with Sharps Safety Features and Maximal Barrier Precautions; Product Code: ASK-04018-OH1
  • Z-1972-2018 · Apr 11, 2018 · Terminated
    Radial Artery Catheterization Kit with Sharps Safety Features; Product Codes: ASK-04020-RIHM
  • Z-1330-2018 · Dec 22, 2017 · Terminated
    (1) Arterial Catheterization Kit, Part Number (PN): ASK-04018-CC; (2) Arterial Line Kit with Sharps Safety Features, PN: ASK-04510-HUM; (3) Arterial Line Kit with Sharps Safety Fea
  • Z-1286-2018 · Oct 26, 2017 · Terminated
    Radial Artery Catheterization Kit; Model: AK-04220
  • Z-1282-2018 · Oct 26, 2017 · Terminated
    Radial Artery Catheterization Kit; Model: AK-04020
  • Z-1281-2018 · Oct 26, 2017 · Terminated
    Radial Artery Catheterization Kit; Model: AK-04018
  • Z-1285-2018 · Oct 26, 2017 · Terminated
    Radial Artery Catheterization Kit; Model: AK-04122
  • Z-1284-2018 · Oct 26, 2017 · Terminated
    Radial Artery Catheterization Kit; Model: AK-04120

…and 17 more.

Other Wire, guide, catheter devices

All Wire, guide, catheter devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.