ARROW IPN040032Recalls & reported problems
Teleflex Incorporated · StimuCath(R) Continuous Peripheral Nerve Block Set · Class 2
All models of ARROW (1494)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 20801902033158), received between Feb 23, 2022 and Feb 23, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (1 report).
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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Break1
- Difficult to Remove1
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.
MalfunctionFeb 23, 2022Break; Difficult to Remove; Break; Difficult to Remove
ONE OF MY COLLEAGUES PLACED ABOVE TYPE OF NERVE CATHETER IN A PATIENTS AT OUR (B)(6) ORTHOPEDIC AND ARTHRITIC CENTER SITE. SHE WAS D/C WITH HOME WITH THE NERVE CATHETER AS USUAL FOR PATIENTS ENROLLED IN OUR HOME CATHETER PROGRAM. WHEN TRYING TO REMOVE THE CATHETER HERSELF (AS PER OUR PRACTICE), THE CATHETER BROKE. THE DISTAL END WAS SUBSEQUENTLY REMOVED IN ER BY OUR APS. THIS IS AN ISOLATED INCIDENT AND HAS NEVER HAPPENED BEFORE AT THE IN MY KNOWLEDGE IN OUR PRACTICE BUT I DO TRUST YOU WOULD LIKELY TO BE MADE AWARE OF THIS INCIDENT. ADDITIONAL INFORMATION: THE METAL WIRE AND ATTACHED COILED TIP WERE REMOVED WITH GENTLE TRACTION BY ONE OF OUR ANESTHESIOLOGISTS.
Patient problems: Foreign Body In Patient
MAUDE report 13586718 ↗
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 405735Becton, Dickinson And Company · Anesthesia conduction kit1 recall3 reports
- BD Luer-Lok, BD Glaspak 405609Becton, 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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page