MAUDE Adverse Event Report: SORIN GROUP DEUTSCHLAND S5 GAS BLENDER; GAS CONTROL UNIT, CARDIOPULMONARY BYPASS

Model Number 25-40-45

Device Problem Other (for use when an appropriate device code cannot be identified) (2203)

Patient Problem No Consequences Or Impact To Patient (2199)

Event Date 08/22/2013

Event Type  Other  

Event Description

During a routine preventative maintenance visit at a customer facility by a sorin group service rep, the perfusionist reported that the s5 gas blender had not maintained the set flow rate during recent set-ups and procedures.The clinician would reset the flow rate to correct the problem and there had been no pt consequences.

Manufacturer Narrative

(b)(4).Sorin group service rep, the perfusionist reported that the s5 gas blender had not maintained the set flow rate during recent set-ups and procedures.The clinician would reset the flow rate to correct the problem and there had been no pt consequences.The blender has been replaced.The investigation is ongoing.A f/u report will be sent when the investigation is complete.

• Brand Name: S5 GAS BLENDER
• Type of Device: GAS CONTROL UNIT, CARDIOPULMONARY BYPASS
• Manufacturer (Section D): SORIN GROUP DEUTSCHLAND; lindberghstr. 25; munich D 80 939; GM D 80939
• Manufacturer (Section G): SORIN GROUP DEUTSCHLAND; lindberghstr. 25; munich D 80 939; GM D 80939
• Manufacturer Contact: cheri voorhees, mgr. ; 14401 w. 65th way; arvada, CO 80004 ; 3034676527
• MDR Report Key: 3592679
• MDR Text Key: 19726927
• Report Number: 1718850-2013-00316
• Device Sequence Number: 1
• Product Code: DTX
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K101046
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Health Professional
• Reporter Occupation: Other
• Remedial Action: Other
• Type of Report: Initial
• Report Date: 12/10/2013

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: 25-40-45
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Initial Date Manufacturer Received: 12/10/2013
• Initial Date FDA Received: 01/06/2014
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 06/01/2011
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Reuse
• Patient Sequence Number: 1