Sechrist Industries, Inc. 3600E-00Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00852682007934), received between Sep 1, 2026 and Sep 1, 2026 — classified as 1 injury.

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.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjurySep 1, 2026Adverse Event Without Identified Device or Use Problem

  Patient problems: Cardiac Arrest

  MAUDE report 50550121 ↗

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