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ARROW IPN032686Recalls & reported problems

Teleflex Incorporated · ARTERIAL ACCESS TRAY · 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 00801902098269), received between Jul 10, 2024 and Jul 10, 2024 — classified as 1 malfunction.

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

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. 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: 1 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: 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 Puncture/Hole1
  • Unsealed Device Packaging1

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.

  • MalfunctionJul 10, 2024Unsealed Device Packaging; Material Puncture/Hole; Unsealed Device Packaging; Material Puncture/Hole

    IT WAS REPORTED THAT: "HOLES WERE FOUND IN PACKAGING. STERILITY WAS COMPROMISED. THE ISSUE WAS IDENTIFIED PRIOR TO USE, THERE WAS NO PATIENT INVOLVEMENT." THIS COMPLAINT IS FOR A LARGE QUANTITY OF 50 DEVICES WITH THE SAME ISSUE, IDENTIFIED AT THE SAME TIME PRIOR TO USE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 19709082 ↗

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-1972-2018 · Apr 11, 2018 · Terminated
    Radial Artery Catheterization Kit with Sharps Safety Features; Product Codes: ASK-04020-RIHM
  • Z-1969-2018 · Apr 11, 2018 · Terminated
    Arterial Line Kit with Sharps Safety Features and Maximal Barrier Precautions; Product Code: ASK-04018-OH1
  • Z-2019-2018 · Apr 11, 2018 · Terminated
    Arterial Catheterization Kit; Product Code:NA-04550-1A
  • 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-1970-2018 · Apr 11, 2018 · Terminated
    Radial Artery Catheterization Kit; Product Codes: ASK-04020-AH, ASK-04020-MIHS, ASK-04120-HF1
  • 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-1281-2018 · Oct 26, 2017 · Terminated
    Radial Artery Catheterization Kit; Model: AK-04018
  • Z-1283-2018 · Oct 26, 2017 · Terminated
    Radial Artery Catheterization Kit; Model: AK-04020-C
  • Z-1286-2018 · Oct 26, 2017 · Terminated
    Radial Artery Catheterization Kit; Model: AK-04220
  • Z-1284-2018 · Oct 26, 2017 · Terminated
    Radial Artery Catheterization Kit; Model: AK-04120
  • Z-1282-2018 · Oct 26, 2017 · Terminated
    Radial Artery Catheterization Kit; Model: AK-04020

…and 17 more.

Other WIRE, GUIDE, CATHETER devices

All WIRE, GUIDE, CATHETER devices →

Sources and updates

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