Sechrist Monoplace Hyperbaric Chamber with Electronic recall: Software Issue
Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module Model 3300E/ER The Hyperbaric Chamber is intended to provide 100% oxygen to the…
Why was Sechrist Monoplace Hyperbaric Chamber with Electronic 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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Serial Numbers: 330001-330069, 330071, 330072, 330074, 330075.
- Product
- Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module Model 3300E/ER The Hyperbaric Chamber is intended to provide 100% oxygen to the…
- Recalling firm
- Sechrist Industries Inc
- Quantity
- 73 units
- Distribution
- Worldwide Distribution - USA (nationwide) and the countries of Bulgaria, and Canada
- Recall date
- November 14, 2012
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)