Sechrist Industries, Inc. 3300H-00Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00852682007637), received between Jan 31, 2025 and Jan 31, 2025 — classified as 1 death, 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJan 31, 2025Use of Device Problem; Insufficient Device Problem Information; Use of Device Problem; Insufficient Device Problem Information

  ON (B)(6) 2025, SECHRIST BECAME AWARE OF A DEATH, TO A CHILD, THAT WAS BEING TREATED IN A HYPERBARIC CHAMBER. HIS MOM, WHO WAS NEXT TO THE CHAMBER AT THE TIME, ALSO SUFFERED INJURIES TO HER ARMS. OFFICIALS IN TROY, MICHIGAN ARE INVESTIGATING THE MATTER.

  Patient problems: Insufficient Information

  MAUDE report 21289215 ↗
• DeathJan 31, 2025Use of Device Problem; Insufficient Device Problem Information; Use of Device Problem; Insufficient Device Problem Information

  ON JANUARY 31, 2025, SECHRIST BECAME AWARE OF A DEATH, TO A CHILD, THAT WAS BEING TREATED IN A HYPERBARIC CHAMBER. OFFICIALS IN (B)(6), MICHIGAN CONFIRMED A CHILD DIED AFTER THE INCIDENT.

  Patient problems: Burn(s); Insufficient Information

  MAUDE report 21289171 ↗