Anesthesia Support TrayRecalls & reported problems across all models
B. Braun Medical Inc. · 3 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one Anesthesia Support Tray model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 1
We found 3 models of Anesthesia Support Tray by B. Braun Medical Inc. in the FDA's device registry (GUDID). Together they are named in 6 adverse event reports in the FDA's MAUDE database, received between Sep 10, 2018 and Jun 4, 2025 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Contamination /Decontamination Problem” (6 reports).
1 FDA recall record name at least one of these models by its device identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Anesthesia Support Tray recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- May 25, 2022Open, Classified
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.
Z-1616-2022 · Root cause: Environmental control · Recall details · FDA record ↗
Most reported Anesthesia Support Tray problems
Device problems
- Contamination /Decontamination Problem6
Patient problems
- No Clinical Signs, Symptoms or Conditions5
- No Consequences Or Impact To Patient1
Anesthesia Support Tray models
3 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Anesthesia Support Tray 332116Anesthesia conduction kit1 recall1 report
- Anesthesia Support Tray 332112Anesthesia conduction kit4 reports
- Anesthesia Support Tray 332114Anesthesia conduction kit1 report
Recent Anesthesia Support Tray adverse event reports
The 6 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionJun 4, 2025Contamination /Decontamination Problem; Contamination /Decontamination Problem
AS REPORTED BY THE USER FACILITY: OUR TECHS HAVE NOTICED SOME MOISTURE INSIDE THE 10 ML SYRINGES IN OUR KITS FROM B BRAUN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22141131 ↗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 ↗MalfunctionSep 10, 2018Contamination /Decontamination Problem; Contamination /Decontamination Problem
AS REPORTED BY THE USER FACILITY: END USER STATED THAT HER STAFF IS NOTICING EITHER INCREASED MOISTURE OR EXCESS LUBRICANT ON THE INSIDE OF THE SYRINGES. IT WAS STATED THAT IT SEEMS LIKE ITS LUBRICANT. NO INJURY REPORTED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7859870 ↗
Other B. Braun Medical Inc. products
- Infusomat54 models · 2,783 reports · 30 recalls
- IV Administration Set153 models · 281 reports · 68 recalls
- Hemodialysis Bloodlines9 models · 2,179 reports · 14 recalls
- Outlook25 models · 195 reports · 24 recalls
- Perifix57 models · 224 reports · 20 recalls
- Extension Set41 models · 101 reports · 16 recalls
- Design Options116 models · 132 reports · 14 recalls
- Blood Administration Set24 models · 177 reports · 13 recalls
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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.
How reports and recalls are matched · Editorial policy · Report an error on this page