Sechrist Industries, Inc. 3600H-00-0Recalls & reported problems
Sechrist Industries, Inc. · HBO CHMBR,ASSY,36IN,ENGLISH,BLUE,CLASSIC · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00899660002079), received between Aug 18, 2025 and Aug 18, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fail-Safe Did Not Operate” (1 report).
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
- Fail-Safe Did Not Operate1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 18, 2025Fail-Safe Did Not Operate; Fail-Safe Did Not Operate
CUSTOMER REPORTED THE CHAMBER DOOR OPENED AT 5 PSI DURING DAILY STARTUP AND CHECK. NO PATIENT INJURY WAS REPORTED. CUSTOMER WOULD LIKE THE CHAMBER CHECKED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22835445 ↗
Other Chamber, Hyperbaric devices
- Sechrist Industries, Inc. 3200-00Sechrist Industries, Inc. · Chamber, Hyperbaric4 reports
- Sechrist Industries, Inc. 3600HR-00-1Sechrist Industries, Inc. · Chamber, Hyperbaric2 reports
- Sechrist Industries, Inc. 3600ER-00Sechrist Industries, Inc. · Chamber, Hyperbaric2 reports
- Sechrist Industries, Inc. 3300H-00Sechrist Industries, Inc. · Chamber, Hyperbaric1 death2 reports
- Sechrist Industries, Inc. 4100HRP-01-1Sechrist Industries, Inc. · Chamber, Hyperbaric1 report
- Sechrist Industries, Inc. 3600H-H-01-1Sechrist Industries, Inc. · Chamber, Hyperbaric1 report
- Sechrist Industries, Inc. 3600E-00Sechrist Industries, Inc. · Chamber, Hyperbaric1 report
- Vitaeris 320 15C37179Hyperbaric Technologies, Inc. · Chamber, Hyperbaric1 report
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.
How reports and recalls are matched · Editorial policy · Report an error on this page