Sechrist Industries, Inc. 3500CP-G4Recalls & reported problems
Sechrist Industries, Inc. · MIXER,GENERAL,GERMAN · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00899660002796), received between Oct 30, 2024 and Feb 18, 2025 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Device Contamination with Body Fluid” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Device Contamination with Body Fluid2
- No Audible Alarm1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 18, 2025Device Contamination with Body Fluid; Device Contamination with Body Fluid
EU DISTRIBUTOR INFORMING SECHRIST OF CUSTOMER REPORTING " BLOOD INSIDE AND SEVERAL COMPONENTS HEAVILY CORRODED." NO PATIENT/ USER INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21406894 ↗MalfunctionDec 11, 2024Device Contamination with Body Fluid; Device Contamination with Body Fluid
DURING PM SERVICE BY A THIRD PARTY, THE MIXER WAS DISCOVERED TO BE CONTAMINATED WITH BLOOD ON THE INSIDE AND THEREFORE DETERMINED TO BE DEFECTIVE. NO PATIENT INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20904359 ↗MalfunctionOct 30, 2024No Audible Alarm; No Audible Alarm
CUSTOMER REPORTED, "GAS SHORTAGE ALARM NOT WORKING. AS THE ALARM IS NOT WORKING, DOES THIS MEAN THERE IS NO AUDIBLE SIGNAL? IF SO, COULD IT BE THAT THE FOLLOWING OCCURRED AND THEREFORE THE ALARM WAS MISSING: WARNING: THE GAS MIXER AUDIBLE ALARM MAY NOT FUNCTION WHEN BOTH AIR AND OXYGEN INLET PRESSURES ARE LESS THAN THE MINIMUM SPECIFIED INLET PRESSURE OF 30 PSIG."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20571130 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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