MAUDE Adverse Event Report: ARJOHUNTLEIGH INC. KINAIR MEDPULSE

Model Number 409000

Device Problems Device Inoperable (1663); Defective Component (2292)

Patient Problems No Known Impact Or Consequence To Patient (2692); No Information (3190)

Event Date 11/03/2014

Event Type  malfunction  

Event Description

Initially it has been claimed that the side rail was broken and keeps falling down.Although the bed was malfunctioning it remained in service and was still being used.As far there are no records of any patient injury which resulted from the side rail failure.

Manufacturer Narrative

(b)(4).As a consequence of issue with the integration of the former (b)(4) into arjohuntleigh and challenges from i.E.It perspective we were forced to a more manual process to screen service data for complaints.We have realized that this process did not detect all complaints and that arjohuntleigh have failed to get them all timely into our complaint handling system.Unfortunately, as a result of a retrospective review after this finding we have identified this reportable complaint that is filed late.As a consequence of the complaint being old we have limited information on the event while additional effort to obtain data has been performed.We will continue our efforts to complete this investigation.A capa has been initiated to document the efforts to complete investigations, and implement corrects and corrective actions.Additional information will be provided upon conclusion of the investigation.

• Brand Name: KINAIR MEDPULSE
• Manufacturer (Section D): ARJOHUNTLEIGH INC.; 12625 wetmore rd ste 308; san antonio TX 78247
• Manufacturer (Section G): ARJOHUNTLEIGH INC.; 12625 wetmore rd ste 308; san antonio TX 78247
• Manufacturer Contact: pamela wright ; 12625 wetmore rd ste 308; san antonio, TX 78247 ; 2102787040
• MDR Report Key: 4652069
• MDR Text Key: 5680829
• Report Number: 3009988881-2015-00029
• Device Sequence Number: 1
• Product Code: INX
• Combination Product (y/n): N
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: User Facility
• Reporter Occupation: Other
• Remedial Action: Inspection
• Type of Report: Initial
• Report Date: 11/03/2014

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: Other
• Device Model Number: 409000
• Was Device Available for Evaluation?: Yes
• Initial Date Manufacturer Received: 11/03/2014
• Initial Date FDA Received: 04/01/2015
• Was Device Evaluated by Manufacturer?: No
• 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
• Patient Outcome(s): Other