UTERINE MANIPULATOR - 7CM
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
(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.
(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.
(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.
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 |