FDA Adverse Event Malfunction Summary report: N

UNKNOWN_MEDICAL_PRODUCT

MDR report key: 3140409 · Received May 31, 2013

Report

Report Number
0001831750-2013-04950
Event Type
Malfunction
Date Received
May 31, 2013
Date of Event
May 7, 2013
Report Date
May 7, 2013
Manufacturer
STRYKER MEDICAL-KALAMAZOO
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CO, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

FOLLOW-UP SUBMITTED AS IT WAS DETERMINED AN INSPECTION WAS ALLEGEDLY PERFORMED BY THE CUSTOMER NOTING THE FOOT END LIFT WAS STUCK IN AN ELEVATED POSITION. WHEN CONTACTED, CUSTOMER STATED THEY HAD ALREADY PERFORMED THE REPAIR. EVALUATION PERFORMED BY CUSTOMER.

Additional Manufacturer Narrative · 1

FOLLOW-UP SUBMITTED AS IT WAS DETERMINED THIS COMPLAINT WAS PREVIOUSLY REPORTED IN MEDWATCH #0001831750-2013-04955.

Additional Manufacturer Narrative · 1

MANUFACTURER¿S INVESTIGATION IS STILL ONGOING; IF ADDITIONAL INFORMATION IS RECEIVED, A FOLLOW-UP REPORT WILL BE SUBMITTED.

Description of Event or Problem · 1

IT WAS REPORTED VIA REPAIR WORK ORDER THAT THE FOOT END LIFT WAS STUCK ELEVATED. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

Description of Event or Problem · 1

IT WAS REPORTED VIA REPAIR WORK ORDER THAT THE FOOT END LIFT WAS STUCK ELEVATED. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

Description of Event or Problem · 1

IT WAS REPORTED VIA REPAIR WORK ORDER THAT THE FOOT END LIFT WAS STUCK ELEVATED. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
241646 UNKNOWN_MEDICAL_PRODUCT BED, AC-POWERED ADJUSTABLE HOSPITAL FNL STRYKER MEDICAL-KALAMAZOO

Patients

Seq Age Sex Outcome Treatment
1