MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-01-14 for MODULAR CATHCART BALL 49MM OD 1363-49-000 136349000 manufactured by Depuy Orthopaedics Inc Us.
[175033729]
(b)(4). 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
[175033730]
The patient was revised to address pain. Doi: unknown; dor: (b)(6) 2019 (unknown hip).
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1818910-2020-01732 |
MDR Report Key | 9586828 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2020-01-14 |
Date of Report | 2019-12-30 |
Date of Event | 2019-12-30 |
Date Mfgr Received | 2020-02-14 |
Device Manufacturer Date | 2018-07-31 |
Date Added to Maude | 2020-01-14 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | KARA DITTY-BOVARD |
Manufacturer Street | 1210 WARD AVENUE |
Manufacturer City | WEST CHESTER IN 465810988 |
Manufacturer Country | US |
Manufacturer Postal | 465810988 |
Manufacturer Phone | 6103142063 |
Manufacturer G1 | JJM (SUZHOU) LTD. 3006356043 |
Manufacturer Street | NO.299 CHANGYANG ST SUZHOU INDUSTRIAL PARK |
Manufacturer City | SUZHOU JIANGSU 21512-6 |
Manufacturer Country | CH |
Manufacturer Postal Code | 21512-6 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | MODULAR CATHCART BALL 49MM OD |
Generic Name | HEMI HIP IMPLANT : HIP ACETABULAR METAL HEMI |
Product Code | LZY |
Date Received | 2020-01-14 |
Model Number | 1363-49-000 |
Catalog Number | 136349000 |
Lot Number | D18072747 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
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 | 2020-01-14 |