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, ClassifiedDescription/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, ClassifiedFLEXTIP 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, ClassifiedArrow 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 · TerminatedFlexTip Plus Epidural Catheterization Kit, Product Code AK-05500
- Z-1172-2020 · Jan 15, 2020 · TerminatedFlexTip Plus Epidural Catheterization Kit, Product Code AK-05501
- Z-1174-2020 · Jan 15, 2020 · TerminatedFlexTip Plus Epidural Catheterization Kit, Product Code ASK-02220-SRH
- Z-1236-2020 · Dec 20, 2019 · TerminatedArrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05400-CA1
- Z-1237-2020 · Dec 20, 2019 · TerminatedArrow FlexTip Plus(R) Epidural Catheterization Kit ASK-17019-MSC
- Z-1238-2020 · Dec 20, 2019 · TerminatedArrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05500-CAN
Other CATHETER, CONDUCTION, ANESTHETIC devices
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- ARROW IPN924999Teleflex Incorporated · CATHETER, CONDUCTION, ANESTHETIC3 recalls0 reports
- ARROW IPN924964Teleflex Incorporated · CATHETER, CONDUCTION, ANESTHETIC2 recalls1 report
- ARROW IPN927743Teleflex Incorporated · CATHETER, CONDUCTION, ANESTHETIC2 recalls0 reports
- ARROW IPN922619Teleflex Incorporated · CATHETER, CONDUCTION, ANESTHETIC2 recalls0 reports
- ARROW IPN924975Teleflex Incorporated · CATHETER, CONDUCTION, ANESTHETIC2 recalls0 reports
- ARROW IPN925052Teleflex Incorporated · CATHETER, CONDUCTION, ANESTHETIC2 recalls0 reports
- ARROW IPN925020Teleflex Incorporated · CATHETER, CONDUCTION, ANESTHETIC2 recalls0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.