FDAFDA · Food and drugs·Recall number Z-0209-2013
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
Published November 14, 2012 · Recall initiated: August 28, 2008
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Telephone
Recall details
- Manufacturer
- Sechrist Industries Inc
- Distributor
- Worldwide Distribution - USA (nationwide) and the countries of Bulgaria, and Canada
- Lot
- Serial Numbers: 360001-360049, 360051-360064, 360068.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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