MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-03-16 for REDAPT 71354757 manufactured by Smith Nephew, Inc..
        [183507264]
This is another case for this patient who developed another peri prosthetic fracture. Patient was doing well with physical therapy using a walker at home as needed. He returned to md office 2 months post-surgery with complaints of pain at right hip area. X-ray completed in office and reveals a fracture of the plate and revision surgery was scheduled 4 days later. During this or procedure, the femoral component of the original surgery was replaced with a new smith and nephew fracture plate implanted and would cultures were done. Wound culture were negative. Device information: synthes plate (noted in emr as "plate fem prox ss lcp" 4. 5mm 10h 283mm lgth rt).
 Patient Sequence No: 1, Text Type: D, B5
| Report Number | 9834930 | 
| MDR Report Key | 9834930 | 
| Date Received | 2020-03-16 | 
| Date of Report | 2020-03-04 | 
| Date of Event | 2020-01-10 | 
| Report Date | 2020-03-04 | 
| Date Reported to FDA | 2020-03-04 | 
| Date Reported to Mfgr | 2020-03-16 | 
| Date Added to Maude | 2020-03-16 | 
| Event Key | 0 | 
| Report Source Code | User Facility report | 
| Manufacturer Link | N | 
| Number of Patients in Event | 0 | 
| Adverse Event Flag | 3 | 
| Product Problem Flag | 3 | 
| Reprocessed and Reused Flag | 3 | 
| Reporter Occupation | RISK MANAGER | 
| Health Professional | 3 | 
| Initial Report to FDA | 3 | 
| Report to FDA | 3 | 
| Event Location | 3 | 
| Single Use | 3 | 
| Previous Use Code | 3 | 
| Event Type | 3 | 
| Type of Report | 3 | 
| Brand Name | REDAPT | 
| Generic Name | PROSTHESIS, HIP, SEMI-CONSTRAINED, UNCEMENTED, METAL/POLYMER, NON-POROUS | 
| Product Code | KTW | 
| Date Received | 2020-03-16 | 
| Model Number | 71354757 | 
| Catalog Number | 71354757 | 
| Device Availability | Y | 
| Device Age | DA | 
| Device Eval'ed by Mfgr | * | 
| Device Sequence No | 1 | 
| Device Event Key | 0 | 
| Manufacturer | SMITH NEPHEW, INC. | 
| Manufacturer Address | 1303 GOSHEN PKWY WEST CHESTER PA 19380 US 19380 | 
| Patient Number | Treatment | Outcome | Date | 
|---|---|---|---|
| 1 | 0 | 1. Other | 2020-03-16 |