Sechrist Industries, Inc. 3500CP-G24Recalls & reported problems
Sechrist Industries, Inc. · MIXER,GENERAL,GERMAN MAQUET · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 00852682007491), received between Mar 5, 2025 and Mar 31, 2026 — classified as 4 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 Flow1
- Unintended System Motion1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- Abnormal Blood Gases1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 31, 2026No Flow
CUSTOMER REPORTED THE SECHRIST BLENDER DOES NOT DELIVER THE DESIRED AMOUNT OF OXYGEN. NO PATIENT INCIDENT WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24749996 ↗MalfunctionAug 15, 2025Device Contamination with Body Fluid; Device Contamination with Body Fluid
EU DISTRIBUTOR INFORMING SECHRIST OF MIXER HIGHLY CONTAMINATED WITH BLOOD AND CORROSISON. NO PATIENT INVOLVEMENT OR INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22820312 ↗MalfunctionJun 26, 2025Unintended System Motion; Unintended System Motion
THE CUSTOMER REPORTED THE FOLLOWING, "THE PATIENT ON VA ECMO WAS STABLE BUT SUDDEN CHANGE IN SPO2 PROMPTED REASSESSMENT OF THE PATIENT AND EQUIPMENT. GAS DELIVERY WAS UNIMPAIRED, HOWEVER IT WAS NOTED THAT THE AIR-OXYGEN BLENDER DIAL WAS FREELY ROTATING AROUND THE ROTARY PIN., AND COULD EASILY BE REMOVED. IT WAS NOT CLEAR WHAT FIO2 WAS BEING DELIVERED TO THE HLS MODULE. THE EQUIPMENT WAS REMOVED FROM SERVICE AND HYPOXIA RESOLVED WITH O2 DELIVERED VIA WALL SUPPLY (FIO2 1.0)."
Patient problems: Abnormal Blood Gases
MAUDE report 22340458 ↗MalfunctionMar 5, 2025Device Contamination with Body Fluid; Device Contamination with Body Fluid
EU DISTRIBUTOR INFORMING SECHRIST OF CUSTOMER REPORTING "BLOOD INSIDE MIXER AND SEVERAL COMPONENTS HEAVILY CORRODED." NO PATIENT/USER INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21529721 ↗
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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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