MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,other report with the FDA on 2020-03-04 for PROFEMUR? MODULAR FEMORAL NECK PHA01202 manufactured by Microport Orthopedics Inc..
[182524482]
Allegedly, patient was revised due to poly wear+pain without loosening components not revised: tige "anca fit? " rev. Hap 1/3 proximal 17. 5d, ppr67628, lot r0797645. 1.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3010536692-2020-00188 |
MDR Report Key | 9788874 |
Report Source | FOREIGN,OTHER |
Date Received | 2020-03-04 |
Date of Report | 2020-03-04 |
Date Facility Aware | 2019-07-02 |
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 | 0 |
Initial Report to FDA | 0 |
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 | PROFEMUR? MODULAR FEMORAL NECK |
Generic Name | HIP COMPONENT |
Product Code | LWJ |
Date Received | 2020-03-04 |
Model Number | PHA01202 |
Catalog Number | PHA01202 |
Lot Number | V08215418 |
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 |