MAUDE Adverse Event Report: KING SYSTEMS ADULT ANESTHESIA CIRCUIT

Catalog Number 8604B-96Z

Device Problems False Reading From Device Non-Compliance (1228); Leak/Splash (1354)

Patient Problem No Known Impact Or Consequence To Patient (2692)

Event Date 04/13/2012

Event Type  malfunction  

Event Description

Leaking co2 line causing false readings.

• Brand Name: ADULT ANESTHESIA CIRCUIT
• Type of Device: ANESTHESIA CIRCUIT
• Manufacturer (Section D): KING SYSTEMS; noblesville IN
• Manufacturer Contact: 15011 herriman blvd.; noblesville, IN 46060 ; 3177766823
• MDR Report Key: 4012588
• MDR Text Key: 4781327
• Report Number: 1824226-2014-00013
• Device Sequence Number: 1
• Product Code: CAI
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: EXEMPT
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: User Facility
• Reporter Occupation: Other
• Type of Report: Initial
• Report Date: 06/23/2014

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 06/25/2014
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Catalogue Number: 8604B-96Z
• Device Lot Number: IZWHX
• Was Device Available for Evaluation?: Yes
• Date Returned to Manufacturer: 04/25/2012
• Is the Reporter a Health Professional?: No
• Date Manufacturer Received: 04/13/2012
• Was Device Evaluated by Manufacturer?: Yes
• Date Device Manufactured: 03/19/2012
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1