B.BRAUN 332100Recalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 04046964177408), received between Dec 10, 2018 and Sep 29, 2026 — classified as 7 malfunctions.

The most frequently reported specific device problem is “Contamination /Decontamination Problem” (7 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 29, 2026Contamination /Decontamination Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50927912 ↗
• MalfunctionNov 11, 2025Contamination /Decontamination Problem; Contamination /Decontamination Problem

  AS REPORTED BY THE USER FACILITY: WHEN DR WAS DRAWING UP MEDICATION, THE LIDO 1% AND KEN 40 MG, LEFT A PIECE OF RUBBER IN THE SYRINGE. FORTUNATELY, NOTICED AND IMMEDIATELY GOT RID OF THE SYRINGE. WE GOT ALL NEW SUPPLIES AND MEDICATIONS TO DRAW THE MEDICATIONS UP. NO INJURY REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23524624 ↗
• MalfunctionJun 9, 2020Contamination /Decontamination Problem; Contamination /Decontamination Problem

  PER MEDWATCH NUMBER: (B)(4). EVENT DESCRIPTION: 5CC PLASTIC SYRINGE WAS FOUND TO CONTAIN WHAT APPEARED TO BE A BLACK PARTICLE OF STOPPER. THE PRESENCE OF THIS PARTICLE WAS OBSERVED BY PHYSICIAN PRIOR TO ADMINISTRATION, WHEN TRIAMCINOLONE ACETONIDE INJECTABLE SUSPENSION WAS DRAWN INTO 5CC PLASTIC SYRINGE. NO INJURY REPORTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 10132696 ↗
• MalfunctionMay 15, 2019Contamination /Decontamination Problem; Contamination /Decontamination Problem

  AS REPORTED BY THE USER FACILITY: THE CUSTOMER OPENED A TRAY AND THE SYRINGE HAD A LIQUID SUBSTANCE INSIDE THAT SMEARED WHEN THE PLUNGER WAS MOVED. NO INJURY REPORTED.

  Patient problems: No Patient Involvement

  MAUDE report 8612022 ↗
• MalfunctionDec 10, 2018Contamination /Decontamination Problem; Contamination /Decontamination Problem

  AS REPORTED BY THE USER FACILITY: EVENT 2: COMPLAINT: CUSTOMER STATED THE SYRINGES IN THE PERIPHERAL NERVE BLOCK SUPPORT TRAY HAD "CONDENSATION" IN THEM. THEY APPEARED "CLOUDY". NO INJURY REPORTED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8148480 ↗
• MalfunctionDec 10, 2018Contamination /Decontamination Problem; Contamination /Decontamination Problem

  AS REPORTED BY THE USER FACILITY: EVENT 3: COMPLAINT: CUSTOMER STATED THE SYRINGES IN THE PERIPHERAL NERVE BLOCK SUPPORT TRAY HAD "CONDENSATION" IN THEM. THEY APPEARED "CLOUDY". NO INJURY REPORTED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8148468 ↗
• MalfunctionDec 10, 2018Contamination /Decontamination Problem; Contamination /Decontamination Problem

  AS REPORTED BY THE USER FACILITY: EVENT 1: COMPLAINT: CUSTOMER STATED THE SYRINGES IN THE PERIPHERAL NERVE BLOCK SUPPORT TRAY HAD "CONDENSATION" IN THEM. THEY APPEARED "CLOUDY". NO INJURY REPORTED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8148467 ↗