B.BRAUN 8713112DRecalls & reported problems
B. Braun Medical Inc. · POWER SUPPLY SP US III · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 18
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 18 adverse event reports that list this exact device (DI 04046964085673), received between Jul 18, 2018 and Nov 30, 2022 — classified as 18 malfunctions.
The most frequently reported specific device problem is “Thermal Decomposition of Device” (12 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 16, 2026.
Most reported problems
Device problems
- Thermal Decomposition of Device12
- Temperature Problem6
- Degraded2
- Patient Device Interaction Problem1
Patient problems
- No Consequences Or Impact To Patient8
- No Clinical Signs, Symptoms or Conditions6
- No Known Impact Or Consequence To Patient3
- No Patient Involvement1
Recent adverse event reports
The 18 most recent of 18 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 30, 2022Temperature Problem; Temperature Problem
AS DESCRIBED AS THE USER FACILITY: POWER CORD SUPPLY STOPPED WORKING, LOOKS LIKE POSSIBLE INTERNAL FAULT, ONE OF THE PRONGS SLIGHTLY MELTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15886805 ↗MalfunctionApr 12, 2022Degraded; Temperature Problem; Degraded; Temperature Problem
AS REPORTED BY THE USER FACILITY: EVENT 2 CUSTOMER REPORTED A LOOSE PRONG AND THERMAL DAMAGE ON TWO POWER CORDS. NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14083725 ↗MalfunctionApr 12, 2022Degraded; Temperature Problem; Degraded; Temperature Problem
AS REPORTED BY THE USER FACILITY: EVENT 1. CUSTOMER REPORTED A LOOSE PRONG AND THERMAL DAMAGE ON TWO POWER CORDS. NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14083721 ↗MalfunctionApr 4, 2022Temperature Problem; Temperature Problem
AS REPORTED BY THE USER FACILITY: POWER CORD WITH THERMAL DAMAGE-PHOTO PROVIDED. NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13995094 ↗MalfunctionFeb 8, 2022Temperature Problem; Patient Device Interaction Problem; Temperature Problem; Patient Device Interaction Problem
AS REPORTED BY THE USER FACILITY: PATIENT HEARD A NOISE IN HER ROOM AND SAW THAT THE POWER CORD WAS SMOKING WHILE IN THE ELECTRICAL WALL SOCKET NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13480326 ↗MalfunctionMay 21, 2021Temperature Problem; Temperature Problem
AS REPORTED BY THE USER FACILITY: THE POWER CORD IS "SCORCHED".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11866075 ↗MalfunctionSep 24, 2019Thermal Decomposition of Device; Thermal Decomposition of Device
AS REPORTED BY USER FACILITY: PLASTIC WAS MELTING.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9112502 ↗MalfunctionFeb 13, 2019Thermal Decomposition of Device; Thermal Decomposition of Device
AS REPORTED BY USER FACILITY: BURNT HOT PRONG.
Patient problems: No Patient Involvement
MAUDE report 8335744 ↗MalfunctionDec 12, 2018Thermal Decomposition of Device; Thermal Decomposition of Device
THE POWER SUPPLY WAS ORIGINALLY REPORTED AS DAMAGED. ONCE THE POWER SUPPLY WAS RECEIVED BY B. BRAUN INC. (BBMI) (IMPORTER), IT WAS VISUALLY INSPECTED AND IT WAS DISCOVERED THAT THE POWER SUPPLY EXHIBITED SIGNS OF THERMAL DAMAGE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8154853 ↗MalfunctionDec 12, 2018Thermal Decomposition of Device; Thermal Decomposition of Device
THE POWER SUPPLY WAS ORIGINALLY REPORTED AS DAMAGED. ONCE THE POWER SUPPLY WAS RECEIVED BY (B)(4), IT WAS VISUALLY INSPECTED AND IT WAS DISCOVERED THAT THE POWER SUPPLY EXHIBITED SIGNS OF THERMAL DAMAGE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8154852 ↗MalfunctionJul 19, 2018Thermal Decomposition of Device; Thermal Decomposition of Device
AS REPORTED BY USER FACILITY: HOT PRONG BURNT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7702936 ↗MalfunctionJul 19, 2018Thermal Decomposition of Device; Thermal Decomposition of Device
AS REPORTED BY USER FACILITY: HOT PRONG BURNT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7702928 ↗MalfunctionJul 19, 2018Thermal Decomposition of Device; Thermal Decomposition of Device
AS REPORTED BY USER FACILITY: HOT PRONG BURNT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7702927 ↗MalfunctionJul 19, 2018Thermal Decomposition of Device; Thermal Decomposition of Device
AS REPORTED BY USER FACILITY: HOT PRONG BURNT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7702926 ↗MalfunctionJul 19, 2018Thermal Decomposition of Device; Thermal Decomposition of Device
AS REPORTED BY USER FACILITY: HOT PRONG BURNT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7702918 ↗MalfunctionJul 18, 2018Thermal Decomposition of Device; Thermal Decomposition of Device
AS REPORTED BY USER FACILITY: DAMAGED POWER CORD.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7698046 ↗MalfunctionJul 18, 2018Thermal Decomposition of Device; Thermal Decomposition of Device
AS REPORTED BY USER FACILITY: DAMAGED POWER CORD.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7698037 ↗MalfunctionJul 18, 2018Thermal Decomposition of Device; Thermal Decomposition of Device
AS REPORTED BY USER FACILITY: DAMAGED POWER CORD.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7698034 ↗
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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 14, 2026 · each report above links to its original FDA record
- 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.
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