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Sechrist Industries, Inc. 3200-00Recalls & reported problems

Sechrist Industries, Inc. · HBO CHMBER,32IN,PNMTC,ENGLISH,BLUE · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
4
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00852682007903), received between Mar 3, 2025 and Jan 12, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Key or Button Unresponsive/not Working” (2 reports).

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: 0 reportsMar 2025: 1 reportsApr 2025: 1 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 1 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 1 reportsFeb 2026: 0 reportsMar 2026: 0 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

  • Key or Button Unresponsive/not Working2
  • Fail-Safe Did Not Operate1
  • Protective Measures Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions4

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJan 12, 2026Key or Button Unresponsive/not Working

    CUSTOMER REPORTED THE EMERGENCY VENT BUTTON IS NOT WORKING TO PERFORM EMERGENCY DECOMPRESSION TEST. CUSTOMER ALSO REPORTED THE TIMING IS OUT OF SPEC FOR COMPRESSION. NO PATIENT INCIDENT WAS REPORTED. ISSUE WAS DISCOVERED AT TIME OF ROUTINE TESTING.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24048671 ↗
  • MalfunctionOct 21, 2025Protective Measures Problem; Protective Measures Problem

    CUSTOMER REPORTED THAT DURING PRE-CLINICAL CHECK THE CHAMBER IS FALLING OUTSIDE THE 120 SECOND TIME FRAME TO BE IN SPEC FOR THE EMERGENCY VENTING. NO PATIENT INVOLVEMENT OR PATIENT/USER INJURY REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23353006 ↗
  • MalfunctionApr 18, 2025Fail-Safe Did Not Operate; Fail-Safe Did Not Operate

    DURING PM SERVICE, SECHRIST INDUSTRIES TECHNICIAN DISCOVERED THAT THE EMERGENCY VENT BUTTON WAS NOT WORKING PROPERLY. FACILITY NEVER REPORTED TO SECHRIST. EMERGENCY VENT BUTTON WOULD ONLY WORK WHEN PUSH EM VENT BUTTON AND TURN MASTER VALVE TO EM VENT POSITION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21868147 ↗
  • MalfunctionMar 3, 2025Key or Button Unresponsive/not Working; Key or Button Unresponsive/not Working

    AS REPORTED BY THE CUSTOMER, WHEN DOING WEEKLY CHECKS, NOTICED EMERGENCY VENT BUTTON WAS NOT WORKING PROPERLY. WHEN BUTTON PUSHED AND HELD DOWN THE DECOMPRESSION DID NOT BEGIN, INSTEAD HAD TO PUSH 4 OR 5 TIMES BEFORE DECOMPRESSION STARTED. NO PATIENT INVOLVEMENT OR INJURY REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21509616 ↗

Other Chamber, Hyperbaric devices

All Chamber, Hyperbaric devices →

Sources and updates

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