ECHOBRIGHT* Insulated Echogenic Regional Block Needle 39207Recalls & reported problems
Avanos Medical, Inc. · ECHOBRIGHT* Echogenic Regional Block Needle with Injection Set · Class 2
Data updated Oct 18, 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 00193494392079), received between Jan 28, 2021 and May 16, 2022 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Blocked Connection” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Blocked Connection1
- Priming Problem1
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.
MalfunctionMay 16, 2022Blocked Connection
WHILE ATTEMPTING TO FLUSH THE LINE IN PREPARATION FOR A NERVE BLOCK THE JUNCTION BETWEEN THE NEEDLE AND WHERE IT MEETS THE TUBING IS BLOCKED OFF.
Patient problems: Insufficient Information
MAUDE report 14407120 ↗MalfunctionJan 28, 2021Priming Problem
WHEN NURSES ARE TRYING TO WITHDRAW THE ORDERED REGIONAL BLOCK, PRIOR TO ADMINISTERING TO THE PATIENT, THE NEEDLE DOES NOT ALLOW THE MEDICATION TO BE WITHDRAWN. THERE IS NOT A VISIBLE DEFECT TO THE NAKED EYE THAT CAN BE IDENTIFIED PRIOR TO OPENING THE PACKAGE. NO PATIENT HARM HAS OCCURRED. THE DEFECT HAS BEEN IDENTIFIED WITH THE AVANOS AND THE HALYARD PRODUCT, BUT THE STAFF BELIEVES AVANOS IS NOW THE PARENT COMPANY THEREFORE AVANOS' INFORMATION WILL BE PROVIDED IN THE REPORT. HALYARD DEVICE INFORMATION: REF: (B)(4) (NUMBER APPEARS UNDER REF NUMBER ON PACKAGING), LOT: 30051022, EXP DATE: 3/31/2023, (B)(4).
Patient problems: Insufficient Information
MAUDE report 11243150 ↗
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 Glaspak 405675Becton, 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 18, 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