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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: SECHRIST INDUSTRIES, INC. HYPERBARIC CHAMBER CHAMBER, HYPERBARIC

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SECHRIST INDUSTRIES, INC. HYPERBARIC CHAMBER CHAMBER, HYPERBARIC Back to Search Results
Model Number 3300H
Event Date 04/19/2012
Event Type  Malfunction  
Event Description

Customer reported chamber compression rate is running too fast.

 
Manufacturer Narrative

Service representative sent to site to investigate and repair device. Details shall be provided in a f/u report once they are obtained.

 
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Brand NameHYPERBARIC CHAMBER
Type of DeviceCHAMBER, HYPERBARIC
Manufacturer (Section D)
SECHRIST INDUSTRIES, INC.
anaheim CA
Manufacturer (Section G)
SECHRIST INDUSTRIES, INC.
4225 east la palma ave.
anaheim CA 92807
Manufacturer Contact
4225 east la palma ave.
anaheim , CA 92807
7145798400
MDR Report Key2586244
Report Number2020676-2012-00019
Device Sequence Number1
Product CodeCBF
Report Source Manufacturer
Source Type Health Professional
Reporter Occupation RESPIRATORY THERAPIST
Remedial Action Repair
Type of Report Initial
Report Date 05/18/2012
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received05/18/2012
Is This An Adverse Event Report? No
Is This A Product Problem Report? Yes
Device Operator
Device MODEL Number3300H
Device Catalogue Number3300H
Is The Reporter A Health Professional? Yes
Date Manufacturer Received04/19/2012
Was Device Evaluated By Manufacturer? Device Not Returned To Manufacturer
Date Device Manufactured01/27/2011
Is this a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Unkown

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