FDA Adverse Event Injury Summary report: N

PROLIFT PELVIC FLOOR REPAIR UNKNOWN PRODUCT

MDR report key: 7223548 · Received January 26, 2018

Report

Report Number
2210968-2018-70489
Event Type
Injury
Date Received
January 26, 2018
Report Date
January 3, 2018
Manufacturer
ETHICON INC.
Product Code
OTP
PMA / PMN Number
K013718
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). TO DATE THE DEVICE HAS NOT BEEN RETURNED. IF THE DEVICE OR FURTHER DETAILS ARE RECEIVED AT A LATER DATE A SUPPLEMENTAL MEDWATCH WILL BE SENT. CITATION: TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY 51 (2012) 283-284. DOI:10.1016/J.TJOG.2012.04.021

Description of Event or Problem · 1

IT WAS REPORTED IN JOURNAL ARTICLE ¿TITLE: PELVIC FLOOR ABSCESS SECONDARY TO GOSSYPIBOMA FOLLOWING A TOTAL PROLIFT PROCEDURE¿ THAT THE PATIENT UNDERWENT SURGICAL PROCEDURE AND MESH WAS IMPLANTED. THE PATIENT EXPERIENCED MESH EROSION RESULTING FROM GOSSYPIBOMA. THE PATIENT REPORTED INTERMITTENT VAGINAL DISCHARGE AND FEVER DURING THE FIRST POSTOPERATIVE FOLLOW-UP (POSTOPERATIVE DAY 12). PELVIC EXAMINATION SHOWED 1-1.5 CM OF MESH EROSION IN THE MIDLINE OF THE ANTERIOR VAGINA INCISION WITHOUT POP RECURRENCE. ALTHOUGH VAGINAL DOUCHE WITH GENTAMICIN 80MG IN THE OUTPATIENT DEPARTMENT AND 3 COMBINATIONS OF ANTIBIOTICS (METRONIDAZOLE 250MG, SULBACTAM SODIUM/AMPICILLIN SODIUM 375MG, LEVOFLOXACIN 500MG) WERE USED, MALODOR OF VAGINAL DISCHARGE PERSISTED FOR 7 DAYS. THE EXPOSED MESH WAS JUST TRIMMED AND THE VAGINAL MUCOSA WAS RESUTURED DUE TO LIMITED EXPOSURE AREA. MUCH PUS WAS DRAINED SPONTANEOUSLY, AND CULTURED MEDIUM SHOWED ESCHERICHIA COLI COLONIZATION. AFTER 2 WEEKS OF ALLEVIATION FROM FEVER, THE PATIENT REPORTED SOME DISCHARGE COMING OUT OF THE VAGINA AGAIN. AFTER INCISION AND DISSECTION OF THE VAGINAL WOUND, ONE PIECE OF GAUZE WAS SEEN IN THE PARAVESICAL SPACE. THE GAUZE WAS TAKEN OUT AND PART OF THE MESH WAS EXCISED. AFTER DEBRIDEMENT, NO FURTHER FEVER AND MALODOROUS DISCHARGE WAS NOTED. THE PATIENT HAS REMAINED CONTINENT AND FREE OF POP FOR OVER 1 YEAR AT THE TIME OF WRITING. IT WAS REPORTED THAT ¿THERE IS NO DOUBT THAT A RETAINED GAUZE CONTRIBUTED TO POOR HEALING OF THE VAGINAL WOUND FOLLOWING MESH SURGERY, MAKING THE EXPOSURE OF MESH MORE LIKELY¿. NO ADDITIONAL INFORMATION WAS PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
64809 PROLIFT PELVIC FLOOR REPAIR UNKNOWN PRODUCT MESH, SURGICAL, SYNTHETIC, UROGYNECOLOGIC OTP ETHICON INC. UNK

Patients

Seq Age Sex Outcome Treatment
1 67 YR Required Intervention