MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer,other report with the FDA on 2020-03-17 for UNKNOWN HIP FEMORAL STEM UNK HIP FEMORAL STEM manufactured by Depuy Orthopaedics Inc Us.
[184471968]
(b)(4). Initial reporter occupation: lawyer. If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Patient Sequence No: 1, Text Type: N, H10
[184471969]
After review of medical records the patient was revised to address metal on metal right total hip. Indications reported she had increasing metal toxicity with elevated cobalt-chrome levels. Revision note reported metallosis around the right hip. No evidence of loosening of the acetabular component and femoral component. There was minimal trunnionosis on the trunnion. Doi: (b)(6) 2004; dor: (b)(6) 2018 (right hip).
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1818910-2020-08307 |
MDR Report Key | 9843328 |
Report Source | CONSUMER,OTHER |
Date Received | 2020-03-17 |
Date of Report | 2020-02-27 |
Date of Event | 2018-09-14 |
Date Mfgr Received | 2020-02-27 |
Date Added to Maude | 2020-03-17 |
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 Contact | KARA DITTY-BOVARD |
Manufacturer Street | 700 ORTHOPAEDIC DRIVE |
Manufacturer City | WARSAW IN 465810988 |
Manufacturer Country | US |
Manufacturer Postal | 465810988 |
Manufacturer Phone | 6107428552 |
Manufacturer G1 | DEPUY INT'L LTD. 8010379 |
Manufacturer Street | ST ANTHONYS ROAD |
Manufacturer City | LEEDS LS118 DT |
Manufacturer Country | UK |
Manufacturer Postal Code | LS11 8 DT |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | UNKNOWN HIP FEMORAL STEM |
Generic Name | HIP FEMORAL STEM |
Product Code | KXA |
Date Received | 2020-03-17 |
Catalog Number | UNK HIP FEMORAL STEM |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | DEPUY ORTHOPAEDICS INC US |
Manufacturer Address | 700 ORTHOPAEDIC DRIVE WARSAW IN 465810988 US 465810988 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2020-03-17 |