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ARROW IPN040094Recalls & reported problems

Teleflex Incorporated · FlexTip Plus(R) Epidural Catheterization Kit · Class 2

All models of ARROW (1494)

Data updated Oct 18, 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 00801902065926), received between Nov 29, 2024 and Nov 29, 2024 — classified as 1 malfunction.

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

9 other recalls cover devices cleared under the same FDA submission (K140110); 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 18, 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: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 1 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

  • Break1

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.

  • MalfunctionNov 29, 2024Break; Break

    IT WAS REPORTED THAT: "GLASS SYRINGE BROKEN. THE ISSUE WAS IDENTIFIED PRIOR TO USE."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 20809469 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K140110. One submission often covers many models, so check the product and lot details in each record.

  • Z-2371-2026 · Apr 21, 2026 · Open, Classified
    Description/REF: EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05502-VM1; EPIDURAL CATHETERIZATION KIT: 19 GA/AK-05501; EPIDURAL CATHETERIZATION KIT/AK-05502; EPIDURAL CATHETERIZATION K
  • Z-1913-2026 · Mar 11, 2026 · Open, Classified
    FLEXTIP PLUS EPIDURAL CATHETER;FLEXBLOCK CONTINOUS PERIPHERAL NERVE BLOCK CATHETER KIT/SET REF ASK-05502-BSM UDI code: (01)10801902209853(17)270831(11)251210(10)33F25K0409 The Arr
  • Z-2288-2020 · May 8, 2020 · Open, Classified
    Arrow FlexTip Plus Epidural Kit with NRFit Connector, catheter system, Product Codes (US) OT19TAGSK OT19TAGSKA OT19TAPSK OT19TCGLK Product Codes (OUS) AT-05501-NRF OT19HBPSS UM-05
  • Z-1177-2020 · Jan 15, 2020 · Terminated
    FlexTip Plus Epidural Catheterization Kit, Product Code AK-05500
  • Z-1172-2020 · Jan 15, 2020 · Terminated
    FlexTip Plus Epidural Catheterization Kit, Product Code AK-05501
  • Z-1174-2020 · Jan 15, 2020 · Terminated
    FlexTip Plus Epidural Catheterization Kit, Product Code ASK-02220-SRH
  • Z-1238-2020 · Dec 20, 2019 · Terminated
    Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05500-CAN
  • Z-1237-2020 · Dec 20, 2019 · Terminated
    Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-17019-MSC
  • Z-1236-2020 · Dec 20, 2019 · Terminated
    Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05400-CA1

Other CATHETER, CONDUCTION, ANESTHETIC devices

All CATHETER, CONDUCTION, ANESTHETIC devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page