GYNECARE MORCELLEX UNKNOWN PRODUCT
Report
- Report Number
- 2210968-2019-82116
- Event Type
- Death
- Date Received
- May 30, 2019
- Date of Event
- September 9, 2017
- Report Date
- May 7, 2019
- Manufacturer
- ETHICON INC.
- Product Code
- HET
- PMA / PMN Number
- K100280
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA
- Reporter Occupation
- OTHER
Narratives
(B)(4). TO DATE THE DEVICE HAS NOT BEEN RETURNED. IF THE DEVICE OR FURTHER DETAILS ARE RECEIVED AT THE LATER DATE A SUPPLEMENTAL MEDWATCH WILL BE SENT. NO CONCLUSION CAN BE DRAWN AT THIS TIME. SHOULD ADDITIONAL INFORMATION BE OBTAINED, A SUPPLEMENTAL 3500A FORM WILL BE SUBMITTED ACCORDINGLY. THE DEVICE INFORMATION FOR USE UNDER PRECAUTIONS STATES" CAUTION: THE USE OF A LAPAROSCOPIC TISSUE EXTRACTION BAG IS RECOMMENDED FOR THE MORCELLATION OF MALIGNANT TISSUE OR TISSUE SUSPECTED OF BEING MALIGNANT AND FOR TISSUE THAT THE PHYSICIAN CONSIDERS TO BE POTENTIALLY HARMFUL WHEN DISSEMINATED IN A BODY CAVITY. AS MORCELLATION MAY AFFECT ENDOMETRIAL PATHOLOGIC EXAMINATION, PREOPERATIVE EVALUATION OF THE ENDOMETRIUM SHOULD BE CONSIDERED. SHOULD MALIGNANCY BE IDENTIFIED, USE OF THE GYNECARE MORCELLEX¿ TISSUE MORCELLATOR MAY LEAD TO DISSEMINATION OF MALIGNANT TISSUE. IT IS UNKNOWN IF THE ACTUAL DEVICE USED IN THIS PATIENT PROCEDURE WAS IN FACT AN ETHICON MORCELLATOR. THE EVENT INVESTIGATION IS ONGOING.
IT WAS REPORTED BY AN ATTORNEY THAT THE PATIENT UNDERWENT A LAPAROSCOPIC SUPRACERVICAL HYSTERECTOMY PROCEDURE IN 2014 AND THE MORCELLATOR WAS USED. IT WAS ALSO REPORTED THAT THE USE OF THE MORCELLATOR LEAD TO THE PATIENT DEVELOPING CANCER AND HER DEATH ON (B)(6) 2017. NO FURTHER INFORMATION IS AVAILABLE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 449301 | GYNECARE MORCELLEX UNKNOWN PRODUCT | LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES) | HET | ETHICON INC. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Death| R |