B.BRAUN 8713142URecalls & reported problems
B. Braun Medical Inc. · SpaceStation with SpaceCom · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04046963716776), received between Mar 8, 2021 and May 4, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Temperature Problem” (2 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.
Most reported problems
Device problems
- Temperature Problem2
- Device Alarm System1
- Failure to Power Up1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 4, 2023Device Alarm System; Failure to Power Up; Temperature Problem; Device Alarm System; Failure to Power Up; Temperature Problem
AS REPORTED BY THE USER FACILITY: COVER - NOT FUNCTIONING, BLINKING RED LIGHT, AND SMOKING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16872568 ↗MalfunctionMar 8, 2021Temperature Problem; Temperature Problem
AS REPORTED BY USER FACILITY: CONNECTOR F4 IN THE BACK IS BURNT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11436236 ↗
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- Alaris 8015Carefusion 303, Inc. · Pump, infusion2 recalls45 deaths148,093 reports
- BD® Alaris™ Pump Module, Model 8100Carefusion 303, Inc. · Pump, infusion5 recalls30 deaths51,256 reports
- Alaris 8110Carefusion 303, Inc. · Pump, infusion2 recalls4 deaths21,956 reports
- Alaris 8110Carefusion 303, Inc. · Pump, infusion2 recalls2 deaths15,547 reports
- Alaris 8015Carefusion 303, Inc. · Pump, infusion3 recalls6 deaths13,022 reports
- CADD 21-6500-51Icu Medical, Inc. · Pump, infusion2 deaths8,231 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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