MAUDE Adverse Event Report: GENDRON BED, MANUAL

Model Number GENDRON 750LB BED

Device Problem Insufficient Information (3190)

Patient Problem Fall (1848)

Event Date 08/09/2018

Event Type  Injury  

Event Description

Resident fell out of his bed.The resident did not sustainany injuries.This report reflects information received by fda in the form of a notification per 803.22 (b)(2).

• Brand Name: BED, MANUAL
• Type of Device: BED, MANUAL
• Manufacturer (Section D): GENDRON
• MDR Report Key: 17530950
• MDR Text Key: 321134590
• Report Number: MW5137866
• Device Sequence Number: 1
• Product Code: FNJ
• Combination Product (y/n): N
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Voluntary
• Reporter Occupation: Other
• Type of Report: Initial
• Report Date: 08/20/2018

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 08/12/2023
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: No
• Device Model Number: GENDRON 750LB BED
• Patient Sequence Number: 1