MAUDE Adverse Event Report: C.R. BARD, INC. (COVINGTON) -1018233 AJUST ADJUSTABLE SINGLE-INCISION SLING; AJUST® ADJUSTABLE SINGLE-INCISION SLING

Catalog Number BRD700SI

Device Problem Adverse Event Without Identified Device or Use Problem (2993)

Patient Problems Erosion (1750); No Code Available (3191); Dyspareunia (4505)

Event Date 11/16/2010

Event Type  Injury  

Manufacturer Narrative

The investigation is still in progress.Once the investigation is complete a supplemental report will be filed.

Event Description

It was reported that the patient experienced dyspareunia, extrusion of tape into vagina.The patient was treated with topical oestrogens which did not result in re-epithelisation of the vagina and the vaginal portion was removed.

Manufacturer Narrative

The reported event was inconclusive as no sample returned for evaluation.The lot number was unknown.Based on the investigation findings the current manufacturing controls are considered adequate as to detect and segregate any non-conforming unit.The event described could not be confirmed as a manufacturing related issue.The device was not returned for evaluation.The lot number was unknown therefore the device history record could not be reviewed.The instructions for use were found adequate and state the following: "precautions the usual precautions associated with urological procedures should be followed: - an experienced and trained physician must determine - based on thorough preoperative assessment - whether the patient and the underlying condition is suitable for the implant procedure.Additional consideration should be given to use of the implant in patients with a compromised immune system any condition that would compromise healing, or any patient with a history of prior abdominal or pelvic surgeries.Consideration should also be given to the ability of the patient to tolerate the surgical procedure.- accepted surgical practice and precautions must be followed for the management of contaminated or infected wound sites, when the ajust sling system is used.- postoperative bleeding may occur in some patients and must be controlled prior to patient release.- the implant procedure requires diligent attention to anatomical structures and diligent care to avoid injury of large vessels, nerves, bladder, bowel, urethra and any viscera during introducer passage.- anatomical distortion can result from pelvic organ prolapse.If the patient requires cystocele repair, it should be performed prior to the implantation of the sub-urethral sling.- proper placement of the sling implant at the mid-urethra requires that it lie flat with minimal or no tension under the urethra.- the ajust® sling system is intended as a single-use device.Do not resterilize any portion of the ajust® sling system.Reuse and/or repackaging may create a risk of patient or user infection, compromise the structural integrity and/or essential material and design characteristics of the device, which may lead to device failure, and/or lead to injury, illness or death of the patient.- patients should be advised that pregnancy following a sling implant procedure may negatively affect the success of such implant procedure and incontinence may recur.The patient is advised to consult with the physician in case of a planned pregnancy.- the safety and effectiveness of the ajust® sling system implant procedure has not been established for the treatment of stress urinary incontinence in males or children under the age of 18.- cystoscopy can be considered at the physician¿s discretion.- check the integrity of the packaging before use.Do not use the implant or introducers if the packaging is opened or damaged.- as for any implantable material, it is recommended to open the package at the time of implantation.- upon opening the ajust® sling system tray, the components should be carefully transferred into the sterile field.The tray should not be inverted to remove components.- post-operatively the patient should be advised to refrain from heavy lifting, exercise (e.G.Cycling, jogging) and/or intercourse until the physician determines it is suitable for the patient to return to normal activities.Adverse events complications associated with the proper implantation of the ajust sling system may include, but are not limited to: - postoperative hematoma, seroma, abscess or fistula formation, or scarring which may occur following the implant procedure.- urinary retention, bladder outlet obstruction and other voiding dysfunctions.These conditions may be associated with over-correction/typically too much tension placed on the implant.- perforations or lacerations of vessels, nerves, bladder, bowel, urethra, vagina, rectum or any viscera, which may occur during the implantation procedure.- irritation at the operative wound site which may elicit a foreign body response that leads to wound dehiscence, inflammation and/or infection.- extrusion through vaginal epithelium or erosion into surrounding viscera and/or mucosa.- inflammation, sensitization, pain, dyspareunia, scarification, contraction, device migration and failure of the procedure resulting in recurrence of incontinence." h11: section a through f - the information provided by bd represents all of the known information at this time.Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to bd.H3 other text : the device was not returned.

Event Description

It was reported that the patient experienced dyspareunia, extrusion of tape into vagina.The patient was treated with topical estrogens which did not result in reepithelisation of the vagina and the vaginal portion was removed.

• Brand Name: AJUST ADJUSTABLE SINGLE-INCISION SLING
• Type of Device: AJUST® ADJUSTABLE SINGLE-INCISION SLING
• Manufacturer (Section D): C.R. BARD, INC. (COVINGTON) -1018233; 8195 industrial blvd; covington 30014
• MDR Report Key: 11324148
• MDR Text Key: 231712905
• Report Number: 1018233-2021-00485
• Device Sequence Number: 1
• Product Code: PAH
• Combination Product (y/n): N
• PMA/PMN Number: K092607
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: health professional,other
• Type of Report: Initial,Followup
• Report Date: 02/22/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 02/12/2021
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Catalogue Number: BRD700SI
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 02/22/2021
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention