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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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 1 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 1 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

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 · Terminated
    Sechrist 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 · Terminated
    Sechrist 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

All Chamber, Hyperbaric devices →

Sources and updates

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