MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2011-01-24 for JOHNSON & JOHNSON M SERIES 85-3635 manufactured by .
[1902706]
Painful left total hip with a loose femoral component - cemented stem. Same pt as (b)(4).
Patient Sequence No: 1, Text Type: D, B5
Report Number | MW5019144 |
MDR Report Key | 1972754 |
Date Received | 2011-01-24 |
Date of Report | 2011-01-24 |
Date of Event | 2002-02-23 |
Date Added to Maude | 2011-02-02 |
Event Key | 0 |
Report Source Code | Voluntary report |
Manufacturer Link | N |
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 | 0 |
Event Location | 0 |
Single Use | 0 |
Previous Use Code | 0 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | JOHNSON & JOHNSON |
Generic Name | CEMENTED FEMORAL COMPONENT |
Product Code | JDI |
Date Received | 2011-01-24 |
Catalog Number | M SERIES 85-3635 |
Lot Number | 1006598 |
Device Availability | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Brand Name | DEPUY |
Generic Name | FEMORAL CEMENT RESTRICTOR |
Product Code | JDK |
Date Received | 2011-01-24 |
Catalog Number | 5460-14-000 |
Lot Number | W1XA21092 |
Device Availability | N |
Device Sequence No | 2 |
Device Event Key | 0 |
Manufacturer | DEPUY ORTHOPAEDICS, INC. |
Manufacturer Address | WARSAW IN 46581 US 46581 |
Brand Name | ENDURANCE BONE CEMENT |
Generic Name | CEMENTED FEMORAL COMPONENT |
Product Code | LOD |
Date Received | 2011-01-24 |
Catalog Number | 5450 50 000 |
Lot Number | V4SAA4000 |
Device Expiration Date | 2004-11-30 |
Device Availability | N |
Device Sequence No | 3 |
Device Event Key | 0 |
Manufacturer | DEPUY ORTHOPAEDICS, INC. |
Manufacturer Address | WARSAW IN 46581 US 46581 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Hospitalization; 2. Deathisabilit | 2011-01-24 |