MAUDE MDR 25220071

MDR report key
25220071
Report number
1018233-2026-03266
Event key
0
Event type
3
Date of event
2026-05-13
Date received
2026-05-19
Adverse event
1
Product problem
0
Patients in event
0
Reporter occupation
100
Health professional
1
Initial report to FDA
0
Event location
0

Manufacturer Contact#

Contact
BDX XEEROY RADA
Address
8195 INDUSTRIAL BLVD COVINGTON GA 30014 US
Phone
770-770-7707
Report source
M

Devices#

Seq, Brand, Generic table
SeqBrandGenericManufacturerProduct codeModelCatalogLotPMA510(k)ImplantEvaluatedAvailability
166922ALYTE? Y-MESH GRAFTMESH GRAFTC.R. BARD INC. (COVINGTON) -1018233OTOY100HUAQ1825NN
505308ALYTE? Y-MESH GRAFTMESH GRAFTC.R. BARD INC. (COVINGTON) -1018233OTOY100HUAQ1825NN

Patients#

Sequence, Received, Treatment table
SequenceReceivedTreatmentOutcome
12026-05-190O

Event Narratives#

N

Patient 0

THE INVESTIGATION IS STILL IN PROGRESS. ONCE THE INVESTIGATION IS COMPLETE A SUPPLEMENTAL REPORT WILL BE FILED. UDI FORMAT UPDATED WITH AVAILABLE PRODUCT INFORMATION PER GUDID. H11: SECTION A THROUGH F - THE INFORMATION PROVIDED BY BD REPRESENTS ALL 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.

D

Patient 0

IT WAS REPORTED BY THE PATIENT'S ATTORNEY THAT AS A RESULT OF HAVING THE PRODUCT IMPLANTED, THE PATIENT HAS EXPERIENCED VAGINAL MESH EXPOSURE, MESH EROSION, VAGINAL PAIN, DISCOMFORT AND TISSUE DAMAGE. SYMPTOMATIC PELVIC ORGAN PROLAPSES WITH SECOND-DEGREE UTERINE PROLAPSE, ANTERIOR VAGINAL DEFECT, PARAVAGINAL DEFECT, POSTERIOR VAGINAL DEFECT, AND PERONEAL DEFECT.