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ARROW IPN046629 (REF SJ-05501)Recalls & reported problems

Teleflex Incorporated · Epidural Catheterization Kit with FlexTip Plus(R), Open Tip Single-Port Catheter and Needle Disposal Feature · Class 2

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 00801902013699), received between Jul 2, 2018 and Jul 2, 2018 — classified as 1 injury.

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Break1

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 2, 2018Break

    LABOR PATIENT HAD EPIDURAL INSERTED BY CRNA WITHOUT DIFFICULTY. NO ISSUES DURING LABOR AND AFTER VAGINAL DELIVERY OF HEALTHY BABY. WHEN THE OB RN WENT TO REMOVE THE EPIDURAL CATHETER, IT BROKE, WITH 5 INCHES REMAINING IN THE EPIDURAL SPACE. OB RN NOTED TIP AT END NOT INTACT AND ONE INCH OF TUBING WITHOUT COATING, ONLY WIRE PRESENT.

    Patient problems: Foreign Body In Patient

    MAUDE report 7658228 ↗

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-1236-2020 · Dec 20, 2019 · Terminated
    Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05400-CA1
  • Z-1237-2020 · Dec 20, 2019 · Terminated
    Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-17019-MSC
  • Z-1238-2020 · Dec 20, 2019 · Terminated
    Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05500-CAN

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.