FDA Adverse Event Malfunction Summary report: N

UTERINE MANIPULATOR - 7CM

MDR report key: 2470065 · Received February 27, 2012

Report

Report Number
3005075853-2012-00793
Event Type
Malfunction
Date Received
February 27, 2012
Date of Event
January 31, 2012
Report Date
February 1, 2012
Manufacturer
ETHICON ENDO-SURGERY, LLC.
Product Code
LKF
PMA / PMN Number
K940681
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE DEVICE WAS NOT RECEIVED FOR ANALYSIS; THEREFORE, THE COMPLAINT COULD NOT BE CONFIRMED. WE DID NOT RECEIVE A BATCH NUMBER OR LOT NUMBER SO THEREFORE WE WERE UNABLE TO REVIEW THE MANUFACTURING RECORDS.

Additional Manufacturer Narrative · 1

(B)(4). INFORMATION ANTICIPATED, BUT UNAVAILABLE AT THIS TIME. ADDITIONAL INFORMATION: DID THE ISSUE OCCUR PRE-OPERATIVE OR INTRA-OPERATIVE? ---INTRA-OPERATIVE. WAS THIS THE INITIAL USE OF THE DEVICE? ---YES. HOW LONG HAS THE SURGEON BEEN USING THIS DEVICE? ---NO INFORMATION. WHAT OTHER DEVICES WERE USED IN CONJUNCTION WITH THE DEVICE? ---NO INFORMATION. WAS THE SALES REP PRESENT DURING THE EVENT? ---NO.

Additional Manufacturer Narrative · 1

(B)(4). THE DEVICE RETURNED WAS FOUND TO BE FULLY FUNCTIONAL. BE SURE THAT THE SYRINGE IN PROPERLY SEATED IN THE INFLATION TUBE. A VALID LOT/BATCH NUMBER WAS NOT RECEIVED THEREFORE, THE DEVICE HISTORY REVIEW COULD NOT BE PERFORMED.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING A LAPAROSCOPIC HYSTERECTOMY PROCEDURE, THE BALLOON WAS BURST. ANOTHER DEVICE WAS USED TO COMPLETE THE CASE. THERE WERE NO ADVERSE CONSEQUENCES TO THE PATIENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 UTERINE MANIPULATOR - 7CM LKF ETHICON ENDO-SURGERY, LLC. NA UNK

Patients

Seq Age Sex Outcome Treatment
1