Sechrist Industries, Inc. 3600ER-00Recalls & reported problems
Sechrist Industries, Inc. · HBO CHMBER,36IN,ELECT CNTRL,REVRS,ENGLISH,BLUE · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00899660002468), received between Feb 13, 2025 and Mar 23, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fail-Safe Did Not Operate” (1 report).
2 other recalls cover devices cleared under the same FDA submission (K052713); they may or may not involve this specific model.
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
- Insufficient Device Problem Information1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 23, 2026Fail-Safe Did Not Operate
CUSTOMER REPORTED TO SECHRIST THAT THE CHAMBER DOOR LOCKING PIN IS NOT ENGAGING UNTIL 4.2 PSIG AND WILL RETRACT AT 7.0 PSIG ON DECOMPRESSION. NO PATIENT OR USER INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24665129 ↗MalfunctionFeb 13, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
CUSTOMER REPORTED THE EMERGENCY VENT TOGGLE SWITCH IS BARELY RESPONDING. THE ISSUE WAS DISCOVERED DURING DAILY STAR-UP. NO PATIENT INCIDENT WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21377503 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K052713. One submission often covers many models, so check the product and lot details in each record.
- Z-0209-2013 · Aug 28, 2008 · TerminatedSechrist Monoplace Hyperbaric Chamber with Electronic Control Module Model 3600E/ER The Hyperbaric Chamber is intended to provide 100% oxygen to the patient at greater than ambien
- Z-0208-2013 · Aug 28, 2008 · TerminatedSechrist Monoplace Hyperbaric Chamber with Electronic Control Module Model 3300E/ER The Hyperbaric Chamber is intended to provide 100% oxygen to the patient at greater than ambien
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. 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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