Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module… — Class II medical device recall Z-0208-2013
Terminated recall by Sechrist Industries Inc, reported 2012-11-14, distributed nationwide. Sechrist conducted a field upgrade on the hyperbaulic chambers equipped with Electronic Control Modules in ord
| Recall number | Z-0208-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Sechrist Industries Inc, Anaheim, CA, United States |
| Recall initiated | 2008-08-28 |
| Classified | 2012-11-06 |
| Reported by FDA | 2012-11-14 |
| Terminated | 2012-11-06 |
| Distributed | Nationwide (US) |
| Countries outside the US | BG, CA |
| Quantity | 73 units |
| Reason classes | software |
| Serial numbers | 330001-330069, 330071, 330072, 330074, 330075 |
| Model numbers | 3300E/ER |
Product
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 ambient pressures.
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0208-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.