Sechrist Industries, Inc. 3600HR-00-1Recalls & reported problems
Sechrist Industries, Inc. · HBO CHMBR,ASSY,36IN,RVRS,ENGLISH,BLUE,STORAGE · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00899660002123), received between Apr 8, 2026 and May 5, 2026 — classified as 2 injuries.
The most frequently reported specific device problem is “Pressure 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
- Adverse Event Without Identified Device or Use Problem1
- Pressure Problem1
Patient problems
- Ear Pain2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 5, 2026Adverse Event Without Identified Device or Use Problem
CUSTOMER REPORTED TO SECHRIST THAT NOTED ON A FEW OCCASIONS THE CHAMBER PRESSURE PULSING/WHOOSHING UPON COMPRESSION AT 2.4 ATA, WITH PATIENT COMPLAINTS OF EAR PAIN.
Patient problems: Ear Pain
MAUDE report 25088619 ↗InjuryApr 8, 2026Pressure Problem
CUSTOMER REPORTING TO SECHRIST, "THAT AFTER THEIR CHAMBER WAS SERVICED BY A THIRD-PARTY, THEIR PATIENTS ARE EXPERIENCING BAROTRAUMA DURING TREATMENTS. THIS HAS HAPPENED ON MULTIPLE PATIENTS."
Patient problems: Ear Pain
MAUDE report 24822921 ↗
Other Chamber, Hyperbaric devices
- Sechrist Industries, Inc. 3200-00Sechrist Industries, Inc. · Chamber, Hyperbaric4 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
- Sechrist Industries, Inc. 3600H-00-0Sechrist Industries, 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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