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ARROW IPN035564 (REF CDC-42703-XP1A)Recalls & reported problems

Teleflex Incorporated · Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter, Sharps Safety Features, and Maximal Barrier Precautions · Class 2 · Implant

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
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801902058584), received between Oct 16, 2015 and Oct 16, 2015 — classified as 1 injury.

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

54 other recalls cover devices cleared under the same FDA submission (K071538); 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.

Most reported problems

Device problems

  • Sticking1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryOct 16, 2015Sticking

    AT HOME, THE PATIENT SUFFERED A CARDIAC ARREST. THE PARAMEDICS WERE CALLED AND RESUSCITATED PATIENT. PATIENT WAS BROUGHT TO EMERGENCY DEPARTMENT AND DIAGNOSED WITH POSTERIOR MYOCARDIAL INFARCTION. EMERGENCY DEPARTMENT PHYSICIAN ATTEMPTED TO PLACE A CENTRAL LINE IN THE FEMORAL ARTERY. THE GUIDEWIRE BECAME STUCK IN THE VESSEL. PATIENT BEGAN CODING AGAIN. AFTER RESUSCITATION, PATIENT TAKEN TO CT FOR HEAD CT SCAN AND THEN EMERGENT CRANIOTOMY. NEXT DAY, CARDIOVASCULAR SURGEON REMOVED GUIDEWIRE AT THE BEDSIDE.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 5200512 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K071538. One submission often covers many models, so check the product and lot details in each record.

  • Z-2376-2026 · Apr 21, 2026 · Open, Classified
    Description/REF: CVC/PSI KIT: 2 LUMEN 8 FR X 6 IN/ASK-42802-PLH; CVC KIT: 3-LUMEN 12 FR X 16 CM/AK-12123-F; CVC KIT: 3-LUMEN 12 FR X 20 CM/AK-15123-F; 3L CVC KIT: 7 FR X 16 CM/ASK-
  • Z-1914-2026 · Mar 11, 2026 · Open, Classified
    ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS CATHETER REF ASK-42802-PLH UDI code: (01)10801902133110(17)261231(11)251211(10)33F25L0140 REF ASK-4
  • Z-2123-2026 · Jan 7, 2026 · Open, Classified
    Medline Convenience Kits: 1) KIT TRIPLE LUMEN INSERTION, Model Number: DYNDM1031A
  • Z-0003-2024 · Aug 10, 2023 · Open, Classified
    Arrow Pressure Injectable Arrowg+ard Blue Plus Four-Lumen CVC, REF CDC-45854-P1A; catheter, intravascular, therapeutic, long-term greater than 30 days
  • Z-0002-2024 · Aug 10, 2023 · Open, Classified
    Arrow ErgoPack Complete, Pressure Injectable Arrowg+ard Blue Plus Four-Lumen CVC, REF CDC-42854- PCN1A; catheter, intravascular, therapeutic, long-term greater than 30 days
  • Z-0351-2023 · Oct 27, 2022 · Terminated
    Arrow MAC Two-Lumen Central Venous Access Kit fr use with 7 - 7.5 Fr Catheters, REF ASK-11242-UPM1; catheter introducer
  • Z-0352-2023 · Oct 27, 2022 · Terminated
    Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit, REF numbers: a) ASK-42703-NS, b) ASK-42703-PCCH2, c) ASK-42703-PUPM1, d) ASK-45703-NS, e) ASK-45703-PAU, f) ASK-45703-
  • Z-1604-2022 · May 25, 2022 · Open, Classified
    TELEFLEX LLC Arrow Central Venous Catheter Kit 16, 18 Gauge Multi Lumen Model Number:CDC-45703-XP1A (Model Numbers # IPN035619, IPN036437, IPN922677)
  • Z-1979-2018 · Apr 11, 2018 · Terminated
    Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter, Sharps Safety Features and Maximal Barrier Precautions; Product Code: ASK-15703-LD
  • Z-1994-2018 · Apr 11, 2018 · Terminated
    ARROWg+ard Blue PLUS Pressure Injectable Multi-Lumen CVC Kit; Product Codes: CDC-45703-P1A; CDC-45703-PB1A; CDC-42703-P1A; and CDC-15703-P1A
  • Z-2000-2018 · Apr 11, 2018 · Terminated
    ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous Catheterization Kit; Product Code: ASK-42703-SJH
  • Z-1988-2018 · Apr 11, 2018 · Terminated
    Pressure Injectable ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous Catheterization Kit; Product Codes: ASK-42703-PAM1, ASK-42703-PSHR1, ASK-45703-PNY, ASK-45703-PWHC1
  • Z-1990-2018 · Apr 11, 2018 · Terminated
    Pressure Injectable Two-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features; Product Code: ASK-45802-PHMW
  • Z-1987-2018 · Apr 11, 2018 · Terminated
    Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features; Product Codes: ASK-42703-MHW and ASK-42703-OLL1
  • Z-1980-2018 · Apr 11, 2018 · Terminated
    Pressure Injectable Multi-Lumen Central Venous Catheterization Kit; Product Code: ASK-15703-PHMC

…and 39 more.

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Sources and updates

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