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 2020-03-19 for UNKNOWN BONE CEMENT UNK CEMENT manufactured by Depuy Cmw - 9610921.
[184282747]
(b)(4). If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate. (b)(4).
Patient Sequence No: 1, Text Type: N, H10
[184282748]
The patient was revised to address of loosening of the tibial component in unknown interface. No apparent adherence of cement to the tibia. Films look as though there is a ballooning cyst beneath the tibial tray in the medial proximal tibial metaphysis. Cultures were negative. Depuy cement was used. No surgical delay. Doi: (b)(6) 2017; dor: (b)(6) 2020; right knee.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1818910-2020-08652 |
MDR Report Key | 9855822 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2020-03-19 |
Date of Report | 2020-03-04 |
Date of Event | 2020-03-04 |
Date Mfgr Received | 2020-03-04 |
Date Added to Maude | 2020-03-19 |
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 | MS. 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 CMW - 9610921 |
Manufacturer Street | COMFORD RD |
Manufacturer City | BLACKPOOL FY4 4QQ |
Manufacturer Country | UK |
Manufacturer Postal Code | FY4 4QQ |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | UNKNOWN BONE CEMENT |
Generic Name | BONE CEMENT |
Product Code | LOD |
Date Received | 2020-03-19 |
Catalog Number | UNK CEMENT |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | DEPUY CMW - 9610921 |
Manufacturer Address | CORNFORD RD BLACKPOOL FY4 4QQ UK FY4 4QQ |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2020-03-19 |