MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,consum report with the FDA on 2020-03-16 for PINNACLE PELVIC FLOOR REPAIR KITS M0068317050 831-705 manufactured by Boston Scientific Corporation.
[186617061]
This event was reported by the patient's legal representation. The surgeon is: (b)(6), md. (b)(6) hospital for women ((b)(6) hospital west). (b)(4). The complaint device is not expected to be returned for evaluation; therefore, a failure analysis of the complaint device could not be completed. If any further relevant information is identified, a supplemental medwatch will be filed.
Patient Sequence No: 1, Text Type: N, H10
[186617062]
Note: this manufacturer report pertains to the first of two devices implanted during the same procedure. It was reported to boston scientific corporation that the patient was diagnosed with recurrent cystocele, stress urinary incontinence (sui) and was implanted with a pinnacle pelvic floor repair mesh and an advantage fit mesh on (b)(6) 2008. As reported by the patient's attorney, the patient was diagnosed with pelvic pain, abdominal pain, dyspareunia, and pelvic graft retraction. On (b)(6) 2008, the patient underwent a surgery for revision of the pinnacle device. Boston scientific has been unable to obtain additional information regarding the event to date.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 3005099803-2020-01017 |
| MDR Report Key | 9834143 |
| Report Source | COMPANY REPRESENTATIVE,CONSUM |
| Date Received | 2020-03-16 |
| Date of Report | 2020-03-16 |
| Date of Event | 2008-11-17 |
| Date Mfgr Received | 2020-02-19 |
| Device Manufacturer Date | 2008-02-28 |
| Date Added to Maude | 2020-03-16 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | CAROLE MORLEY |
| Manufacturer Street | 300 BOSTON SCIENTIFIC WAY |
| Manufacturer City | MARLBOROUGH MA 01752 |
| Manufacturer Country | US |
| Manufacturer Postal | 01752 |
| Manufacturer Phone | 5086834015 |
| Manufacturer G1 | FREUDENBERG MEDICAL MIS INC |
| Manufacturer Street | 2301 CENTENNIAL BOULEVARD |
| Manufacturer City | JEFFERSONVILLE IN 47130 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 47130 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | PINNACLE PELVIC FLOOR REPAIR KITS |
| Generic Name | MESH, SURGICAL, SYNTHETIC, UROGYNECOLOGIC, FOR PELVIC ORGAN PROLAPSE, TRANSVAGIN |
| Product Code | OTP |
| Date Received | 2020-03-16 |
| Model Number | M0068317050 |
| Catalog Number | 831-705 |
| Lot Number | 0PD8013102 |
| Device Expiration Date | 2009-01-31 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | BOSTON SCIENTIFIC CORPORATION |
| Manufacturer Address | 300 BOSTON SCIENTIFIC WAY MARLBOROUGH MA 01752 US 01752 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2020-03-16 |