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ARROW IPN914728Recalls & reported problems

Teleflex Incorporated · ARROW(R) PICC with Chlorag+ard(R) Technology · 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 10801902157543), received between Jul 26, 2022 and Jul 26, 2022 — classified as 1 injury.

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

11 other recalls cover devices cleared under the same FDA submission (K112896); 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

  • Material Separation1

Patient problems

  • Foreign Body In Patient1

Recent adverse event reports

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

  • InjuryJul 26, 2022Material Separation; Material Separation

    IT WAS REPORTED THAT "AFTER IMPLANTATION, AT THE FOLLOW-UP X-RAY, THERE WAS A PRESENCE IN THE LUNG THAT RESULTED FROM THE X-RAY. IT WAS DECIDED TO RETRIEVE THE FOREIGN BODY, WHICH TURNED OUT TO BE THE GUIDE WIRE SHEATH THAT WAS LOCATED IN THE PULMONARY ARTERY. THE PATIENT IS FINE AND THE PICC WAS LEFT IN SITU.". IT WAS REPORTED THE FOREIGN BODY WAS RETRIEVED BY VASCULAR SURGERY AND "A CATHETER WITH A LOOP AT THE TIP WAS INTRODUCED, AND UNDER RADIOGRAPHIC CONTROL THE FOREIGN BODY WAS COMPLETELY REMOVED".

    Patient problems: Foreign Body In Patient

    MAUDE report 15107665 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K112896. One submission often covers many models, so check the product and lot details in each record.

  • Z-2378-2026 · Apr 21, 2026 · Open, Classified
    Description/REF: PI PICC: 3: 6FR x 55CM w CHG/ DLX-35563-HPKC; AGBA PICC: 2L 5.5 FR X 45 CM/ASK-44552-ABKB; AGBA PICC/DELTA KIT: 5.5 FR X 55 CM/ASK-45552-MHBV; AGBA PICC: 1L 4.5FR
  • Z-1811-2019 · Apr 23, 2019 · Terminated
    Arrowg+ard Blue Advance PICC Product Code: CDC45541HPK1A
  • Z-1820-2019 · Apr 23, 2019 · Terminated
    Arrow PICC with Chlorag+ard Technology Product Code:PR 45541 HPHNM
  • Z-1819-2019 · Apr 23, 2019 · Terminated
    Arrow PICC with Chlorag+ard Technology Product Code: PR 45541 HPHNL
  • Z-1822-2019 · Apr 23, 2019 · Terminated
    Arrow PICC with Chlorag+ard Technology Product Code:PR 45552 HPHNM
  • Z-1327-2018 · Dec 22, 2017 · Terminated
    Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard Technology, Part Numbers: (1) ASK-45541-RWJ4; (2) ASK-45552-RWJ4
  • Z-0996-2018 · Nov 27, 2017 · Terminated
    Pressure Injectable Multi- Lumen Central Venous Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology Product Usage: The Arrow CVC is indicated to provide short-ter
  • Z-2698-2017 · Jun 12, 2017 · Terminated
    Arrow EVOLUTION Pressure Injectable PICC with Chlorag+ard Antimicrobial and Antithrombogenic Technology
  • Z-2331-2017 · May 9, 2017 · Terminated
    1) Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology The Pressure Injectable PICC with Chlorag+ard Antimicrobial and Antithrombogenic Technology is indicated for
  • Z-1705-2017 · Mar 3, 2017 · Terminated
    The CG+ Arrow PIC Catheters permit venous access to the central circulation through a peripheral vein.
  • Z-0207-2016 · Oct 16, 2015 · Terminated
    ARROW PICC Kit featuring Chlorag+ard Technology Midline Catheterization Kit ARROW Advantage5 Pressure Injectable PICC Kit Arrow Pressure Injectable Arrow PICC powered by Arrow VPS

Other Catheter, intravascular, therapeutic, long-term greater than 30 days devices

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Sources and updates

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