Class II — Sechrist Industries Inc
| Recalling firm | SECHRIST INDUSTRIES, INC. |
|---|---|
| Registered facility | SECHRIST INDUSTRIES, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Sechrist conducted a field upgrade on the hyperbaulic chambers equipped with Electronic Control Modules in order to correct a software bug that could potentially affect the performance of the chamber. |
| Product | 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 ambient pressures |
| Quantity | 65 units total (61 units in the US) |
| Distribution | Worldwide Distribution - USA (nationwide) and the countries of Bulgaria, and Canada |
| Initiated | 2008-08-28 |
| Classified | 2012-11-06 |
| Terminated | 2012-11-06 |
| Recall number | Z-0209-2013 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Sechrist Industries Inc (Z-0209-2013).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/52796/
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