CONTIPLEX® 331758Recalls & reported problems
B. Braun Medical Inc. · Contiplex® Stim Set, 18 Ga. x 4 in. Insulated Tuohy Needle and Stimulating Catheter (SCNB4) · Class 2
All models of CONTIPLEX (10)
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 04046964177088), received between Oct 22, 2019 and Oct 22, 2019 — 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Break1
Patient problems
- Foreign Body In Patient1
- Neuropathy1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 22, 2019Break; Break
AS REPORTED BY THE USER FACILITY: PATIENT CALLED TO REPORT THAT HE SUSTAINED A RETAINED NERVE BLOCK CATHETER DURING A PROCEDURE THAT WAS PERFORMED ON (B)(4) 2019. PER THE PATIENT, HE WAS INFORMED BY THE SURGICAL TEAM THAT AFTER REMOVAL IT WAS NOTED THAT THE CATHETER TIP HAD BROKEN OFF, AND THE "BLACK TIP" WAS MISSING. THERE WERE NO INTERVENTIONS PERFORMED TO THE PATIENT AT THE TIME OF THE EVENT. BUT NOW THE PATIENT IS COMPLAINING OF NEUROTPATHIES TO THE LOWER LEG.
Patient problems: Foreign Body In Patient; Neuropathy
MAUDE report 9220505 ↗
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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
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- 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.
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