GYNECARE MORCELLEX* TISSUE MORCELLATOR
Report
- Report Number
- 2210968-2013-05575
- Event Type
- Malfunction
- Date Received
- May 15, 2013
- Date of Event
- April 2, 2013
- Report Date
- April 25, 2013
- Manufacturer
- ETHICON, INC.
- Product Code
- HET
- PMA / PMN Number
- K100280
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MA, US
- Reporter Occupation
- PHYSICIAN
Narratives
IN ADDITION, A REVIEW OF THE BATCH MANUFACTURING RECORDS WAS CONDUCTED AND THE BATCH MET ALL FINISHED GOODS RELEASE CRITERIA.
(B)(4). CONCLUSION: THE PRODUCT UPON WHICH THIS MEDWATCH IS BASED IS ANTICIPATED. ONCE THE PRODUCT IS RECEIVED, ANY FURTHER INFORMATION DERIVED FROM THE EVALUATION WILL BE SUBMITTED IN A SUPPLEMENTAL 3500A FORM.
CONCLUSION: THE ACTUAL DEVICE INVOLVED IN THIS EVENT WAS RETURNED FOR EVALUATION. THE DEVICE WAS VISUALLY AND FUNCTIONALLY EVALUATED. THE DRIVE CABLE STOPPED ROTATING WHEN THE TRIGGER WAS RELEASED. HOWEVER, THE BLADE FAILED TO ROTATE DURING THE EVALUATION; IT IS LIKELY THAT THE ACCUMULATION OF BLOOD, BODY FLUIDS, AND TISSUE PREVENTED THE DEVICE FROM CONTINUING TO OPERATE AS INTENDED.
IT WAS REPORTED THAT A PATIENT UNDERWENT A LAPAROSCOPIC TOTAL ABDOMINAL HYSTERECTOMY ON (B)(6) 2013. DURING THE PROCEDURE, THE DEVICE OPERATED WITHOUT BEING ACTIVATED. THE SURGEON ATTEMPTED TO USE A DIFFERENT MACHINE BUT THE DEVICE STILL REMAINED ACTIVATED. ANOTHER LIKE DEVICE WAS USED TO COMPLETE THE PROCEDURE WITH NO ADVERSE PATIENT CONSEQUENCES.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 215520 | GYNECARE MORCELLEX* TISSUE MORCELLATOR | LAPAROSCOPE, GYNECOLOGIC | HET | ETHICON, INC. | NA | MT217773 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |