MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor report with the FDA on 2020-03-04 for DYNASTY? BF SHELL 52MM GROUP D DSBFGD52 manufactured by Microport Orthopedics Inc..
[182152233]
This event will be updated once the investigation is complete. Trends will be evaluate.
Patient Sequence No: 1, Text Type: N, H10
[182152274]
Allegedly, the patient underwent a thr and presented pain, diagnosis of loose acetabular cup that was misaligned causing increased leg lengthening. Received a revision where microport cup, liner and screw were removed and replaced with another company's implants. The femoral head was removed and replaced it with a microport implant head. Femoral stem component remained well fixed. C926.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3010536692-2020-00189 |
MDR Report Key | 9788335 |
Report Source | DISTRIBUTOR |
Date Received | 2020-03-04 |
Date of Report | 2020-03-04 |
Date Facility Aware | 2020-02-13 |
Date Mfgr Received | 2020-02-13 |
Date Added to Maude | 2020-03-04 |
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 Street | 5677 AIRLINE ROAD |
Manufacturer City | ARLINGTON TN 38002 |
Manufacturer Country | US |
Manufacturer Postal | 38002 |
Manufacturer Phone | 9018674771 |
Manufacturer G1 | MICROPORT ORTHOPEDICS INC. |
Manufacturer Street | 5677 AIRLINE RD. |
Manufacturer City | ARLINGTON TN 38002 |
Manufacturer Country | US |
Manufacturer Postal Code | 38002 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | DYNASTY? BF SHELL 52MM GROUP D |
Generic Name | HIP COMPONENT |
Product Code | JDL |
Date Received | 2020-03-04 |
Model Number | DSBFGD52 |
Catalog Number | DSBFGD52 |
Lot Number | 1628187 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MICROPORT ORTHOPEDICS INC. |
Manufacturer Address | 5677 AIRLINE RD. ARLINGTON TN 38002 US 38002 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2020-03-04 |