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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: CONMED CORPORATION VCARE VAGINAL-CERVICAL RETRACTOR-ELEVATOR, MEDIUM; VCARE UTERINE MANIPULATOR

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CONMED CORPORATION VCARE VAGINAL-CERVICAL RETRACTOR-ELEVATOR, MEDIUM; VCARE UTERINE MANIPULATOR Back to Search Results
Catalog Number 60-6085-201
Device Problem Difficult to Remove (1528)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Date 01/09/2013
Event Type  malfunction  
Event Description
Report number (b)(4) was found on the fda maude database stating, "while struggling to remove the uterus from the vaginal vault, the vcare manipulator came apart.The balloon at the distal tip separated from the shaft which allowed the colpotomy cup and occluder to slide off the shaft." the maude report stated that this was a product problem report and not an adverse event report; therefore, based on the information available to conmed corporation, no patient injury occurred.The maude report does not have any end-user facility documented, or, any contact information; therefore, conmed is unable to obtain any further information surrounding this reported event.
 
Manufacturer Narrative
This is an fda reportable event due to a sentinel event reported on medwatch 1320894-2012-00099.The device is unable to be returned to conmed corporation for this event was discovered on the fda maude database.The end-user facility or any contact information has not been documented on the maude report and it is impossible to contact the end-user facility; therefore, an investigation on the suspect device will not be conducted.The device in question, vcare, is a disposable, single-use device for manipulation of the uterus and cervix in surgical and diagnostic procedures.The device consists of a manipulator tube having an inflatable balloon at its proximal end and an anatomically configured cannula / handle for maintaining proper attitude of the uterus at the distal end.The vcare incorporates a system of cup-like elevators to provide manipulation of the uterus, and retraction and elevation of the cervix.The conmed vcare is indicated for manipulation of the uterus and injection of fluids or gases during laparoscopic procedures such as laparoscopic assisted vaginal hysterectomy (lavh), total laparoscopic hysterectomy (tlh), minilap, laparoscopic tubal occlusion, or diagnostic laparoscopy and also maintains pneumoperitoneum by sealing the vagina once a colpotomy is performed.A dhr/lhr, device history record/lot history record, review will not be accomplished as the lot number has not been made available.A potential cause of this complaint is application of force during manipulation of the device which exceeded the cervical cone pull off strength capability.A contributing factor may have been not unlocking the locking mechanism and retracting the vaginal cone prior to removal of the device.This factor would increase resistance allowing the vcare shaft to pull through the cervical cone.The risk associated with this complaint is mitigated in the ifu, instructions for use, which states, "prior to removal of the device, ensure the locking mechanism is released via the thumbscrew and swipe a finger around the edge of the vaginal cup to separate the tissue from the cup to prevent tissue damage.Do not use excessive force upon device removal to avoid traumatizing the vaginal canal and/or component detachment.Vaginal delivery of a large uterus may result in patient injury.Morcellation or other methods should be used to reduce the size of the uterus prior to removal through the vaginal canal.Visually inspect vcare on removal from the patient to verify that the device is intact and all forward components (figure #1: 1.Intrauterine balloon, 2.Cervical cup, 3.Vaginal cup, 4.Locking assembly and 5.Thumbscrew) have been retrieved from the patient." the device was not returned for evaluation and the incident is most probably end-user related.The complaint investigation has not identified a manufacturing or component defect and the malfunction has been determined as use related; therefore, corrective action is not warranted at the present time.Conmed corporation is considering this complaint closed.Not yet returned to manufacturer.
 
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Brand Name
VCARE VAGINAL-CERVICAL RETRACTOR-ELEVATOR, MEDIUM
Type of Device
VCARE UTERINE MANIPULATOR
Manufacturer (Section D)
CONMED CORPORATION
525 french road
utica NY 13502 599
Manufacturer (Section G)
CONMED CORPORATION
525 french road
utica NY 13502 599
Manufacturer Contact
stephen casanova, rn, mps
525 french road
utica, NY 13502-5994
3156243463
MDR Report Key3639292
MDR Text Key21449371
Report Number1320894-2014-00017
Device Sequence Number1
Product Code LKF
Combination Product (y/n)N
PMA/PMN Number
K071907
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Other
Reporter Occupation Other
Type of Report Initial
Report Date 02/21/2014
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Catalogue Number60-6085-201
Device Lot NumberUNKNOWN
Was Device Available for Evaluation? No
Initial Date Manufacturer Received 01/28/2014
Initial Date FDA Received02/21/2014
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured10/01/2012
Is the Device Single Use? Yes
Type of Device Usage Unknown
Patient Sequence Number1
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