Halyard 40791Recalls & reported problems
Avanos Medical, Inc. · HALYARD* ON-Q* T-bloc* Needles & Catheter Sets-18-2-Stimulating · 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 10680651407914), received between Jan 19, 2017 and Jan 19, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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
- Break1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 19, 2017Break; Break
FILL VOLUME: NOT APPLICABLE, FLOW RATE: NOT APPLICABLE, PROCEDURE: ANKLE SURGERY, CATHPLACE: POPLITEAL NERVE BLOCK. IT WAS REPORTED THAT WHEN THE CATHETER WAS PULLED OUT FROM THE NEEDLE, IT BECAME STUCK AND THEN SHEARED. THE DOCTOR REMOVED THE ENTIRE DEVICE AND RESTARTED THE BLOCK WITH A NEW DEVICE. THE PATIENT WAS REPORTED TO HAVE NO INJURIES AS A RESULT OF THE PROCEDURE. ADDITIONAL INFORMATION RECEIVED ON 12-JAN-2017 VERIFIED THAT THIS DEVICE IS THE USUAL T-BLOC CATHETER. IT WAS NOTED THAT IT SHEARED WHILE THEY ATTEMPTED REMOVAL OF THE NEEDLE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6263583 ↗
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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.