MAUDE Adverse Event Report: STRYKER STRYKER ZOOM BED; HOSPITAL BED

Model Number 2040

Device Problems Smoking (1585); Power Problem (3010)

Patient Problem No Information (3190)

Event Date 05/19/2015

Event Type  Injury  

Event Description

Power supply in pt bed began emitting smoke which filled the room with smoke.Pt had to be removed and room ventilated after bed was unplugged.This is the 3rd time we have seen the power supply burn up like this without any signs that anything is wrong.

• Brand Name: STRYKER ZOOM BED
• Type of Device: HOSPITAL BED
• Manufacturer (Section D): STRYKER
• MDR Report Key: 4799604
• MDR Text Key: 5830318
• Report Number: MW5042823
• Device Sequence Number: 1
• Product Code: FNL
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Voluntary
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date: 05/20/2015

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 05/20/2015
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: 2040
• Is the Reporter a Health Professional?: Yes
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention
• Patient Age: 50 YR