ARROW IPN040008Recalls & reported problems
Teleflex Incorporated · 19 Ga. x 60 cm StimuCath(R) Continuous Nerve Block Set · Class 2
- 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 00801902028341), received between Apr 7, 2021 and Apr 7, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Unraveled Material” (1 report).
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
- Unraveled Material1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 7, 2021Unraveled Material; Unraveled Material
CATHETER STARTED TO PARTIALLY UNWIND DURING REMOVAL FROM PATIENT'S LEG. SAME MD PLACED/REMOVED CATHETER AND DID NOT ENCOUNTER RESISTANCE UPON PLACEMENT. PLEASE SEE ATTACHED PICTURES. PACKAGING WAS DISCARDED, BUT ALL LOTS ARE THE SAME IN THE LOCATION WHERE THE DEVICE WERE REMOVED. WE DO HAVE THE CATHETER FOR RETURN AND ANALYSIS BY ARROW.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11629969 ↗
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- 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
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.