Anesthesia Support Tray 332112Recalls & reported problems
B. Braun Medical Inc. · ST200 SUP TRAY NO PROC DRUGS,NO EXT.SET · Class 2
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 04046964177484), received between Sep 28, 2022 and Nov 1, 2024 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Contamination /Decontamination Problem” (4 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.
Reports received per month
Most reported problems
Device problems
- Contamination /Decontamination Problem4
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 1, 2024Contamination /Decontamination Problem; Contamination /Decontamination Problem
AS REPORTED BY USER FACILITY: CUSTOMER BELIEVES THE NEEDLE USED FROM THE TRAY IS DE-BORING THE VIALS OF MEDICATIONS THAT ARE BEING USED TO DRAW UP. THE MEDICALS ARE NOT B. BRAUN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20586528 ↗MalfunctionOct 10, 2024Contamination /Decontamination Problem; Contamination /Decontamination Problem
AS REPORTED, DEBRIS IN 3CC AND 5CC SYRINGES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20415893 ↗MalfunctionAug 28, 2024Contamination /Decontamination Problem; Contamination /Decontamination Problem
AS REPORTED BY THE USER FACILITY: BRIEF INQUIRY DESCRIPTION: DEBRIS IN 3CC AND 5CC SYRINGES. DETAILED INQUIRY DESCRIPTION: DEBRIS IN 3CC AND 5CC SYRINGES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20086202 ↗MalfunctionSep 28, 2022Contamination /Decontamination Problem; Contamination /Decontamination Problem
AS REPORTED BY THE USER FACILITY: IT WAS REPORTED THAT THE 27G NEEDLE WAS CONTAMINATED WITH WHAT LOOKS TO BE A GLUE DRIP FROM THE NEEDLE HUB. NO INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15499929 ↗
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.