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ARROW IPN040128Recalls & reported problems

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

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 00801902007698), received between Feb 10, 2022 and Feb 10, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Unsealed Device Packaging” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • 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.

  • MalfunctionFeb 10, 2022Unsealed Device Packaging; Unsealed Device Packaging

    EPIDURAL PACKAGING WAS BROKEN AND DENTED CAUSING THE STERILITY OF THE INSIDE TO BE QUESTIONED. ONE OF THE PACKAGES THE CORNER WAS BROKEN OFF FROM THE DENT. COULD NOT USE ANY OF THE 3 EPIDURAL PACKAGES AS THEY WERE ALL DENTED AND BROKEN.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13507511 ↗

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-1174-2020 · Jan 15, 2020 · Terminated
    FlexTip Plus Epidural Catheterization Kit, Product Code ASK-02220-SRH
  • Z-1172-2020 · Jan 15, 2020 · Terminated
    FlexTip Plus Epidural Catheterization Kit, Product Code AK-05501
  • 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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.