ARROW IPN923213Recalls & reported problems
Teleflex Incorporated · StimuCath(R) Continuous Peripheral Nerve Block Kit · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10801902206180), received between Apr 12, 2023 and Apr 12, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Material Twisted/Bent” (2 reports).
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
- Material Twisted/Bent2
Patient problems
- Insufficient Information2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 12, 2023Material Twisted/Bent; Material Twisted/Bent
REPORTED ISSUE: DURING AN ATTEMPT TO REMOVE THE INNER GUIDEWIRE, THE BLUE END FELL OFF, THE WIRE WAS REMOVED BUT THE CATHETER UNRAVELED AND KINKED TOWARDS THE TIP. THIS OCCURRED TWICE. THE SAME ISSUE OCCURRED WITH ANOTHER PATIENT WITH THE SAME DEVICE LOT. THERE WAS NO INJURY.
Patient problems: Insufficient Information
MAUDE report 16727102 ↗MalfunctionApr 12, 2023Material Twisted/Bent; Material Twisted/Bent
REPORTED ISSUE: DURING AN ATTEMPT TO REMOVE THE INNER GUIDEWIRE, THE BLUE END FELL OFF, THE WIRE WAS REMOVED BUT THE CATHETER UNRAVELED AND KINKED TOWARDS THE TIP. THIS OCCURRED TWICE. THE SAME ISSUE OCCURRED WITH ANOTHER PATIENT WITH THE SAME DEVICE LOT. THERE WAS NO INJURY.
Patient problems: Insufficient Information
MAUDE report 16726859 ↗
Other Anesthesia conduction kit devices
- BD Luer-Lok, BD Glaspak 405671Becton, Dickinson And Company · Anesthesia conduction kit1 recall68 reports
- ARROW IPN922678Teleflex Incorporated · Anesthesia conduction kit2 recalls0 reports
- BD Luer-Lok, BD Glaspak 405672Becton, Dickinson And Company · Anesthesia conduction kit1 recall27 reports
- BD Luer-Lok, BD Glaspak 405673Becton, Dickinson And Company · Anesthesia conduction kit1 recall10 reports
- BD Luer-Lok, BD Glaspak 405637Becton, Dickinson And Company · Anesthesia conduction kit1 recall7 reports
- BD Luer-Lok, BD Glaspak 405707Becton, Dickinson And Company · Anesthesia conduction kit1 recall4 reports
- BD Luer-Lok, BD Glaspak 405609Becton, Dickinson And Company · Anesthesia conduction kit1 recall3 reports
- BD Luer-Lok, BD Glaspak 405735Becton, Dickinson And Company · Anesthesia conduction kit1 recall3 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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