Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module Model 3300E/ER Recalled by Sechrist Industries Inc Due to Sechrist conducted a field upgrade on the hyperbaulic...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Sechrist Industries Inc directly.
Affected Products
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.
Quantity: 73 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Sechrist Industries Inc
Sechrist Industries Inc has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report