GYNECARE MORCELLEX* TISSUE MORCELLATOR
Report
- Report Number
- 2210968-2012-08383
- Event Type
- Malfunction
- Date Received
- December 20, 2012
- Date of Event
- October 23, 2012
- Report Date
- November 27, 2012
- Manufacturer
- ETHICON, INC.
- Product Code
- HET
- PMA / PMN Number
- K100280
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- JA
- Reporter Occupation
- PHYSICIAN
Narratives
(B)(4): THE ACTUAL DEVICE INVOLVED IN THIS EVENT WAS RETURNED FOR EVALUATION. THE DEVICE WAS VISUALLY AND FUNCTIONALLY EVALUATED. THE DEVICE OPERATED AS INTENDED DURING THE EVALUATION. A SHARPNESS TEST WAS CONDUCTED AND IT MET THE REQUIREMENTS.
(B)(4): 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. IN ADDITION, A REVIEW OF THE BATCH MANUFACTURING RECORDS WAS CONDUCTED AND THE BATCH MET ALL FINISHED GOODS RELEASE CRITERIA. THIS IS ONE OF THREE MEDWATCHES BEING SUBMITTED AS THREE DEVICES WERE INVOLVED IN THIS EVENT. SEE ALSO MEDWATCH 2210968-2012-08382 AND MEDWATCH 2210968-2012-08384. THE SAME PATIENT IS REPRESENTED IN EACH MEDWATCH.
IT WAS REPORTED THAT A PATIENT UNDERWENT A MYOMECTOMY ON (B)(6) 2012. DURING THE PROCEDURE, THE ROTATION SPEED OF THE BLADE WAS GETTING SLOW AND THE TRIGGER SWITCH DID NOT WORK PROPERLY. ANOTHER LIKE DEVICE WAS USED. THERE WERE NO ADVERSE PATIENT CONSEQUENCES.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | GYNECARE MORCELLEX* TISSUE MORCELLATOR | LAPAROSCOPE, GYNECOLOGIC | HET | ETHICON, INC. | NA | MT216697 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |