ARROW IPN040037Recalls & reported problems
Teleflex Incorporated · StimuCath(R) Continuous Peripheral Nerve Block Set · 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 20801902126072), received between Jul 15, 2025 and Jul 29, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (2 reports).
1 other recall cover devices cleared under the same FDA submission (K030937); 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.
Reports received per month
Most reported problems
Device problems
- Material Split, Cut or Torn2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 29, 2025Material Split, Cut or Torn; Material Split, Cut or Torn
IT WAS REPORTED THAT: "THE CATHETER HAS BEEN TORN WHEN BEING WITHDRAWN THROUGH THE NEEDLE. IT WAS REMOVED IN ITS ENTIRETY, NO PIECES REMAINED IN THE PATIENT. NO HARM OCCURRED. THE PATIENT DID HAVE TO UNDERGO A SECOND PROCEDURE TO PLACE A NEW CATHETER."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22640791 ↗MalfunctionJul 15, 2025Material Split, Cut or Torn; Material Split, Cut or Torn
IT WAS REPORTED THAT: "THE CATHETER HAS BEEN TORN WHEN BEING WITHDRAWN THROUGH THE NEEDLE. IT WAS REMOVED IN ITS ENTIRETY, NO PIECES REMAINED IN THE PATIENT. NO HARM OCCURRED. THE PATIENT DID HAVE TO UNDERGO A SECOND PROCEDURE TO PLACE A NEW CATHETER."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22508319 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K030937. One submission often covers many models, so check the product and lot details in each record.
- Z-2894-2011 · Jun 17, 2011 · TerminatedArrow ASK-20608-CMC StimuCath Continuous Nerve Block Kit. Arrow International, Inc. Permits placement of catheters next to nerves and nerve plexuses for continuous nerve block a
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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