Sechrist Industries, Inc. 3300HR-01-1Recalls & reported problems
Sechrist Industries, Inc. · HBO CHMBR,ASSY,33IN,RVRS,ENGLISH,WHITE,STORAGE · 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 00899660002062), received between Sep 19, 2025 and Sep 19, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Activation Problem” (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
- Activation Problem1
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.
MalfunctionSep 19, 2025Activation Problem; Activation Problem
CUSTOMER REPORTED THE RED CHAMBER PRESSURE INDICTOR IS NOT WORKING AND THAT ALSO THE DOOR LATCH IS GETTING STUCK AND NOT ALLOWING THE DOOR TO BE OPENED. ISSUE WAS DISCOVERED DURING CLINICAL CHECK AND THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23098678 ↗
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.
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