FDA Adverse Event Malfunction Summary report: N

POWERLED

MDR report key: 9933403 · Received April 7, 2020

Report

Report Number
9710055-2020-00082
Event Type
Malfunction
Date Received
April 7, 2020
Report Date
October 26, 2020
Manufacturer
MAQUET SAS
Product Code
FSY
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
BE
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 0

THE ISSUE IS BEING INVESTIGATED BY MANUFACTURING SITE.

Additional Manufacturer Narrative · 0

GETINGE BECAME AWARE OF AN ISSUE WITH SPRING ARM OF THE POWERLED SURGICAL LIGHT. AS IT WAS STATED BY THE CUSTOMER, AN OIL LEAKAGE FROM THE SPRING ARM WAS NOTICED. THERE WAS NO SERIOUS INJURY REPORTED HOWEVER WE DECIDED TO REPORT THE ISSUE BASED ON THE POTENTIAL AS ANY DROPLETS FALLING OFF INTO STERILE FIELD OR DURING PROCEDURE MIGHT CAUSE A CONTAMINATION. IT WAS ESTABLISHED THAT WHEN THE EVENT OCCURRED, THE SURGICAL LIGHT DID NOT MEET THE MANUFACTURERS SPECIFICATION AS ALTHOUGH NO TECHNICAL MALFUNCTION HAS BEEN FOUND, THE SITUATION WHICH OCCURRED WAS NOT IN ACCORDANCE TO DEVICE SPECIFICATION AND IT CONTRIBUTED TO THE EVENT. THE PROVIDED INFORMATION DID NOT INDICATE THAT THE DEVICE WAS BEING USED FOR PATIENT TREATMENT WHEN THE EVENT TOOK PLACE. DURING THE INVESTIGATION IT WAS FOUND THAT THERE IS NO APPARENT TREND IN THE COMPLAINTS. IN THE INVESTIGATION COURSE THE PRODUCT EXPERTS ESTABLISHED THAT DURING THE ASSEMBLY OF THE SPRING ARMS THE SUPPLIER APPLIES A CREAMED GREASE, WHICH IS TURNING INTO THE LIQUID ABOVE 135°C. GOING FURTHER, THE PHENOMENON DESCRIBED IN THE CASE AT HAND WAS MOST LIKELY CAUSED BY A PRODUCT COMING FROM THE OUTSIDE (E.G. CLEANING AGENT APPLIED IN SPRAY OR WITH A SPONGE, BUT NOT IN COMPLIANCE WITH THE RECOMMENDATIONS GIVEN IN OUR USER MANUALS) AND IT MIXING UP WITH THE GREASE. THIS IS LIKELY TO OCCUR DUE TO THE POSITION OF THIS METAL TONGUE (LOCATED ON THE LOWER PART OF THE SPRING ARM ON THE BUSHING SIDE) WHERE AN EXCESS OF LIQUID CAN BE ACCUMULATED AND CONSEQUENTLY CAN MIX WITH THE GREASE TO TURN INTO A SORT OF GREASY LIQUID. THIS GREASY LIQUID IS FIRST ACCUMULATED IN THE INNER SIDE OF THE TONGUE AND THEN GOES OUT AND FALL. THE SECOND FACTOR COULD BE RELATED TO A COMBINATION OF AIR CONDITIONING AND EXCESS OF OIL AT THE BUSHING LOCATION. TO PREVENT SUCH SITUATION FROM OCCURRENCE, THE CUSTOMER SHOULD FOLLOW THE CLEANING AND DISINFECTION PROCEDURE DESCRIBED IN THE USER MANUAL. WE BELIEVE THE RELATED DEVICES ARE PERFORMING CORRECTLY IN THE MARKET. WE ALSO BELIEVE THAT IF THE MANUFACTURER RECOMMENDATION WOULD HAVE BEEN FOLLOWED THE INCIDENT WOULD HAVE BEEN AVOIDED.

Additional Manufacturer Narrative · 0

THE ISSUE IS BEING INVESTIGATED BY MANUFACTURING SITE.

Additional Manufacturer Narrative · 0

THE ISSUE IS BEING INVESTIGATED BY MANUFACTURING SITE.

Description of Event or Problem · 0

MANUFACTURER REFERENCE NUMBER (B)(4).

Description of Event or Problem · 0

MANUFACTURER'S REFERENCE NUMBER (B)(4).

Description of Event or Problem · 0

MANUFACTURER REFERENCE NUMBER OT (B)(4).

Description of Event or Problem · 0

MANUFACTURER REFERENCE NUMBER (B)(4).

Additional Manufacturer Narrative · 1

ADDITIONAL INFORMATION WILL BE PROVIDED UPON RESULTS OF INVESTIGATION. DEVICE NOT RETURNED TO MANUFACTURER.

Description of Event or Problem · 1

ON (B)(6) 2020 GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF SURGICAL LIGHTS. AS IT WAS STATED, THE OIL LEAKAGE ON THE SPRING ARM WAS NOTICED. THERE WAS NO INJURY REPORTED HOWEVER WE DECIDED TO REPORT THE ISSUE IN ABUNDANCE OF CAUTION AND BASED ON THE POTENTIAL AS ANY OIL DROPLETS FALLING OFF INTO STERILE FIELD OR DURING PROCEDURE MAY LEAD TO CONTAMINATION. MANUFACTURER'S REFERENCE NUMBER: (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
397010 POWERLED LIGHT, SURGICAL, CEILING MOUNTED FSY MAQUET SAS ARD567910901

Patients

Seq Age Sex Outcome Treatment
1