MAUDE Adverse Event Report: C.R. BARD, INC. (COVINGTON) -1018233 AVAULTA SOLO SYNTHETIC SUPPORT SYSTEM - POSTERIOR; AVAULTA SOLO® SYNTHETIC SUPPORT SYSTEM - POSTERIOR

Catalog Number 486200

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

Patient Problems Abdominal Pain (1685); Rheumatoid Arthritis (1724); Asthma (1726); Erosion (1750); Cyst(s) (1800); Emotional Changes (1831); Incontinence (1928); Itching Sensation (1943); Nausea (1970); Pain (1994); Sepsis (2067); Urinary Tract Infection (2120); Abnormal Vaginal Discharge (2123); Vomiting (2144); Burning Sensation (2146); Hernia (2240); Peritonitis (2252); Distress (2329); Discomfort (2330); Arthralgia (2355); Neck Pain (2433); Prolapse (2475); Intermenstrual Bleeding (2665); Dysuria (2684); Constipation (3274); Dyspareunia (4505); Skin Inflammation/ Irritation (4545); Urinary Incontinence (4572)

Event Type  Injury  

Manufacturer Narrative

The reported event could not be confirmed.No sample was returned for evaluation.Based on the investigation findings, current manufacturing controls are considered adequate as to detect and segregate any non-conforming unit.Event described could not be confirmed as a manufacturing related issue.The alleged event is most likely associated with possible procedural/surgical complications.The ifu currently addresses potential risks associated with surgically implantable materials which states the following: precautions: based on physician experience and training, a thorough assessment of each patient should be made to determine their suitability 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 infected or contaminated wounds.Postoperative bleeding may occur in some patients and must be controlled prior to patient release.Avaulta solo¿ synthetic support system implantation procedures require diligent attention to anatomical structures and care to avoid puncture of large vessels, nerves, bladder, bowel, urethra, rectum, or any viscera during introducer passage.The avaulta solo¿ synthetic support system is provided in a sterile blister tray within a sterile pouch.The sterile blister tray may be placed in the sterile field.The introducers provided with the anterior and posterior synthetic support systems are provided in a sterile blister tray.Transfer the introducer to the sterile field using aseptic techniques.Do not place the tray in the sterile field.Check the integrity of the packaging before use.Do not use the mesh or introducers if the packaging is opened or damaged.As for any implantable material, it is recommended to open the blister tray at the time of implantation.The avaulta solo¿ synthetic support system is intended as a single-use device.Do not re-sterilize any portion of the avaulta solo¿ synthetic support 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.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 reactions: complications associated with the proper implantation of the avaulta solo¿ synthetic support may include, but are not limited to those typically associated with surgically implantable materials, including: postoperative hematoma, seroma, abscess or fistula formation, or scarring which may occur following the implant procedure.Urinary retention, bladder outlet obstruction and other voiding and defecatory dysfunctions.These conditions may be associated with over-correction/too much tension placed on the implant.Perforations or lacerations of vessels, nerves, bladder, bowel, urethra, 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 vaginal wall prolapse.Urinary incontinence (stress and urge).2120, 1994, 1928="l".2329, 1724, 1726, 1970="nl".No sample received.

Event Description

It was reported by the patient's attorney that as a result of having the product implanted, the patient has experienced pain, suffering, disability and impairment.Product was used for therapeutic treatment.Per additional information received, the patient has experienced vaginal bleeding, stabbing pain, mesh erosion, vaginal itching, burning, painful urination, dyspareunia, discomfort, could not play with grandchildren (emotional changes), discharge, leg and abdominal weakness (weakness), erosion through muscle, blood loss, chronic constipation, cystocele (prolapse), hernias, peritonitis/sepsis (infection), rectocele (prolapse), vaginal vault prolapse, uterine prolapse, urinary incontinence, recurrent vaginal pain, and required additional surgical and non-surgical interventions.Per additional information received on 11oct2021, the patient has experienced vaginal bleeding, stabbing pain, mesh erosion, mesh cutting through the muscle tissue, vaginal itching, burning sensation and painful while urination, dyspareunia, inability to perform normal activities, emotional distress, infections, severe pressure and lifting sensation in abdomen, vaginal discharge, leg and abdominal weakness, spotting, mesh exposure, chronic constipation, recurrent cystocele, hernia, rheumatoid arthritis, sepsis, recurrent rectocele, vaginal vault prolapse, uterine prolapse, urinary incontinence, recurrent vaginal pain, celiac disease, unspecified hypothyroidism, unspecified asthma, osteoarthrosis, pelvic pressure, dysuria, chronic urinary tract infections, nausea, vomiting, , neck pain, tarlov¿s cyst, abdominal pain, arthritis, arthralgia, hyperlipidemia, palpitations, irregular sensation in chest, allergic rhinitis, chronic cough, back pain, hip pain, thyroid disease, irritation and required additional surgical and non-surgical interventions.

• Brand Name: AVAULTA SOLO SYNTHETIC SUPPORT SYSTEM - POSTERIOR
• Type of Device: AVAULTA SOLO® SYNTHETIC SUPPORT SYSTEM - POSTERIOR
• Manufacturer (Section D): C.R. BARD, INC. (COVINGTON) -1018233; 8195 industrial blvd; covington GA 30014
• Manufacturer (Section G): C.R. BARD, INC. (COVINGTON) -1018233; 8195 industrial blvd; covington GA 30014
• Manufacturer Contact: yonic anderson ; 8195 industrial blvd; covington, GA 30014 ; 7707846100
• MDR Report Key: 12675285
• MDR Text Key: 278094533
• Report Number: 1018233-2021-80072
• Device Sequence Number: 1
• Product Code: OTP
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K082571
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: other
• Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date: 10/21/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 10/21/2021
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Expiration Date: 11/01/2012
• Device Catalogue Number: 486200
• Device Lot Number: HUUK1833
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: No
• Device Age: 8 MO
• Event Location: Hospital
• Date Manufacturer Received: 10/11/2021
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 01/29/2011
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention
• Patient Age: 52 YR
• Patient Weight: 86