Sechrist Industries Inc: Medical Device Recall in 2012 - (Recall #: Z-0209-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: August 28, 2008

Date Posted: November 14, 2012

Recall Number: Z-0209-2013

Event ID: 52796

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.

Status: Terminated

Product Quantity: 65 units total (61 units in the US)

Code Information:

Serial Numbers: 360001-360049, 360051-360064, 360068.

Distribution Pattern:

Worldwide Distribution - USA (nationwide) and the countries of Bulgaria, and Canada

Voluntary or Mandated:

Voluntary: Firm initiated