Design Options® 570245Recalls & reported problems
B. Braun Medical Inc. · PNB/Support Tray · Class 2
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 04046964526664), received between Jun 6, 2019 and Mar 9, 2022 — classified as 2 injuries, 3 malfunctions.
The most frequently reported specific device problem is “Break” (5 reports).
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
- Break5
Patient problems
- Foreign Body In Patient3
- No Known Impact Or Consequence To Patient2
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjuryMar 9, 2022Break; Break
AS REPORTED BY THE USER FACILITY: EVENT 1: BRIEF INQUIRY DESCRIPTION "BROKEN NERVE BLOCK CATHETER". DETAILED INQUIRY DESCRIPTION TWICE NOW THIS PRODUCT HAS BROKEN OFF IN A PATIENT. NO INJURY REPORTED.
Patient problems: Foreign Body In Patient
MAUDE report 13710205 ↗InjuryMar 9, 2022Break; Break
AS REPORTED BY THE USER FACILITY: EVENT 2: BRIEF INQUIRY DESCRIPTION "BROKEN NERVE BLOCK CATHETER" DETAILED INQUIRY DESCRIPTION TWICE NOW THIS PRODUCT HAS BROKEN OFF IN A PATIENT. NO INJURY REPORTED.
Patient problems: Foreign Body In Patient
MAUDE report 13709857 ↗MalfunctionMar 9, 2022Break; Break
AS REPORTED BY THE USER FACILITY: CATHETER TIP RETAINED IN PATIENT. NO INJURY REPORTED.
Patient problems: Foreign Body In Patient
MAUDE report 13709665 ↗MalfunctionJun 6, 2019Break; Break
AS REPORTED BY THE USER FACILITY: EVENT 2: A CATHETER CONNECTOR DID NOT STAY CLOSED. NO INJURY REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8674571 ↗MalfunctionJun 6, 2019Break; Break
AS REPORTED BY THE USER FACILITY: EVENT 1: A CATHETER CONNECTOR DID NOT STAY CLOSED. NO INJURY REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8674568 ↗
Other Anesthesia conduction kit devices
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- 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.