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
- 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, ClassifiedDescription/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, ClassifiedArrow 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, ClassifiedArrow 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 · TerminatedRadial Artery Catheterization Kit; Product Codes: ASK-04020-AH, ASK-04020-MIHS, ASK-04120-HF1
- Z-1971-2018 · Apr 11, 2018 · TerminatedArterial Catheterization Kit; Product Codes: ASK-04020-DH
- Z-1968-2018 · Apr 11, 2018 · TerminatedRadial Arterial Access Kit; Product Code: ASK-04001-BID2
- Z-2019-2018 · Apr 11, 2018 · TerminatedArterial Catheterization Kit; Product Code:NA-04550-1A
- Z-1969-2018 · Apr 11, 2018 · TerminatedArterial Line Kit with Sharps Safety Features and Maximal Barrier Precautions; Product Code: ASK-04018-OH1
- Z-1972-2018 · Apr 11, 2018 · TerminatedRadial 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 · TerminatedRadial Artery Catheterization Kit; Model: AK-04220
- Z-1282-2018 · Oct 26, 2017 · TerminatedRadial Artery Catheterization Kit; Model: AK-04020
- Z-1281-2018 · Oct 26, 2017 · TerminatedRadial Artery Catheterization Kit; Model: AK-04018
- Z-1285-2018 · Oct 26, 2017 · TerminatedRadial Artery Catheterization Kit; Model: AK-04122
- Z-1284-2018 · Oct 26, 2017 · TerminatedRadial Artery Catheterization Kit; Model: AK-04120
…and 17 more.
Other Wire, guide, catheter devices
- HI-TORQUE BALANCE MIDDLEWEIGHT UNIVERSAL II 1009664Abbott Vascular Inc. · WIRE, GUIDE, CATHETER321 reports
- SYNCHRO 14 M00313010Stryker Corporation · WIRE, GUIDE, CATHETER2 recalls220 reports
- PressureWire™ C12059Lightlab Imaging, Inc. · WIRE, GUIDE, CATHETER1 death296 reports
- SYNCHRO 2 M00326410Stryker Corporation · WIRE, GUIDE, CATHETER2 recalls155 reports
- ENROUTE .014" Guidewire 11686-01Silk Road Medical, Inc. · Wire, Guide, Catheter2 deaths228 reports
- ARROW IPN035915Teleflex Incorporated · WIRE, GUIDE, CATHETER217 reports
- OmniWire Pressure guide wire 89185Philips Image Guided Therapy Corporation · Wire, Guide, Catheter1 recall1 death160 reports
- ARROW IPN055780Teleflex Incorporated · Wire, guide, catheter4 recalls0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.