MAUDE Adverse Event Report: UNKNOWN BED; BED, AC-POWERED ADJUSTABLE HOSPITAL

Device Problem Intermittent Loss of Power (4016)

Patient Problem Insufficient Information (4580)

Event Type  malfunction  

Event Description

On january 27, 2012, stryker medical was notified of a potentially reportable complaint involving a product for which stryker is not the manufacturer.The customer reported one of their beds had intermittent power and it was determined this was due to an issue with a non-stryker manufactured/supplied power cord.Please find additional contact information below.N/a this report reflects information received by fda in the form of a notification per 803.22 (b)(2).

• Brand Name: BED
• Type of Device: BED, AC-POWERED ADJUSTABLE HOSPITAL
• Manufacturer (Section D): UNKNOWN
• MDR Report Key: 17527359
• MDR Text Key: 321332314
• Report Number: MW5134291
• Device Sequence Number: 1
• Product Code: FNL
• 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: 02/23/2012

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
• Patient Sequence Number: 1