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Spinocan® 333214Recalls & reported problems

B. Braun Medical Inc. · Spinocan® 25 Ga. x 3-1/2 in. (90 mm) Tray (Kit) · Class 2

All models of Spinocan (7)

Data updated Oct 18, 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 04046964179426), received between May 5, 2023 and May 5, 2023 — 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 18, 2026.

Most reported problems

Device problems

  • Break1

Patient problems

  • Foreign Body In Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMay 5, 2023Break; Break

    AS REPORTED BY THE USER FACILITY: INSERTED THE CATHETER THROUGH THE INDUCER, IT DID NOT DO WHAT IT WAS SUPPOSED TO DO AND WHEN HE PULLED BACK THE TIP OF THE CATHETER WAS GONE. PATIENT HAD A SURGICAL PROCEDURE WITH A SMALL INCISION TO PULL OUT THE CATHETER PIECE. NO INJURY REPORTED.

    Patient problems: Foreign Body In Patient

    MAUDE report 16875471 ↗

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Sources and updates

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