ClearanceBrief
Recall Z-0208-2013 ยท CBF Chamber, Hyperbaric

Sechrist Industries Inc

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.

DateNov 6, 2012 (initiated Aug 28, 2008)
StatusTerminated
ReasonSechrist 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.
Root causeSoftware design
ActionSechrist Industries contacted consignees by phone to notify them of a software upgarde and to schedule appointments to perform the required field upgrades. An approximate summary of the phone notification is provided below. "I am contacting you to notify you of a field upgrade we are performing on our hyperbaric chambers equipped with Electronic Control Modules in order to correct a software bug that could potentially affect the performance of your chamber. The upgrade includes the installation of a new motherboard with revised software, a reset switch, and the exchange of other control panel
Quantity73 units
DistributionWorldwide Distribution - USA (nationwide) and the countries of Bulgaria, and Canada
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K052713MODEL 3300E/ER MONOPLACE HYPERBARIC OXYGEN CHAMBER
Sechrist Industries, Inc., Oct 28, 2005