MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer,other report with the FDA on 2020-03-30 for UNKNOWN HIP ACETABULAR CUP UNK HIP ACETABULAR CUP manufactured by Depuy Orthopaedics Inc Us.
[186791133]
(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
[186791134]
Pinnacle mom litigation and additional information record received. Litigation alleges injury, pain, weakness, increase sensitivity to metallic ions, emotional distress and difficulty with simple daily activities. Doi: (b)(6) 2009: dor: (b)(6) 2018: left hip.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1818910-2020-09569 |
MDR Report Key | 9897794 |
Report Source | CONSUMER,OTHER |
Date Received | 2020-03-30 |
Date of Report | 2019-04-23 |
Date of Event | 2018-05-24 |
Date Mfgr Received | 2020-03-05 |
Date Added to Maude | 2020-03-30 |
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 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 ORTHOPAEDICS, INC. 1818910 |
Manufacturer Street | 700 ORTHOPAEDIC DR. |
Manufacturer City | WARSAW IN 465810988 |
Manufacturer Country | US |
Manufacturer Postal Code | 465810988 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | UNKNOWN HIP ACETABULAR CUP |
Generic Name | HIP ACETABULAR CUP |
Product Code | KWA |
Date Received | 2020-03-30 |
Catalog Number | UNK HIP ACETABULAR CUP |
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 | 2020-03-30 |