Sechrist Industries, Inc. 3300HR-01-0Recalls & reported problems
Sechrist Industries, Inc. · HBO CHMBR,ASSY,33IN,RVRS,ENGLISH,WHITE,CLASSIC · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00899660002055), received between May 14, 2025 and May 14, 2025 — classified as 1 injury.
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
Patient problems
- Cramp(s) /Muscle Spasm(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 14, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
CUSTOMER REPORTED TO SECHRIST THAT SEVERAL PATIENTS HAVE COMPLAINED OF SEVERE CRAMPING AFTER COMING OUT OF THE CHAMBER. CUSTOMER DID NOT REPORT ANY ISSUES WITH THE CHAMBER. THEY REQUESTED SECHRIST COME OUT AND EVALUATE THE CHAMBER ANYWAY. THEY WERE ALSO GOING TO CONTACT THE SUPPLIER OF THEIR MEDICAL GAS FOR A PURITY REPORT.
Patient problems: Cramp(s) /Muscle Spasm(s)
MAUDE report 22021872 ↗
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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