FDA Adverse Event Injury Summary report: N

TOTAL HIP BALL 28MM +5

MDR report key: 1020285 · Received March 25, 2008

Report

Report Number
1818910-2008-00977
Event Type
Injury
Date Received
March 25, 2008
Date of Event
March 12, 2008
Report Date
March 12, 2008
Manufacturer
DEPUY ORTHOPAEDICS, INC.
Product Code
JDI
PMA / PMN Number
K860701
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NC, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

EXAMINATION WAS NOT POSSIBLE, AS THE DEVICES WERE NOT RETURNED. REVIEW OF THE DEVICE HISTORY RECORDS WAS ALSO NOT POSSIBLE AS THE LOT CODES REQUIRED FOR RETRIEVAL WERE UNAVAILABLE. THE INVESTIGATION COULD NOT VERIFY OR IDENTIFY ANY EVIDENCE OF PRODUCT ERROR WITH REGARD TO THE REPORTED EVENT WITH THE INFO AVAILABLE. BASED ON THE INVESTIGATION, THE NEED FOR CORRECTIVE IS NOT INDICATED.

Description of Event or Problem · 1

THE PT WAS REVISED BECAUSE OF DISLOCATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTAL HIP BALL 28MM +5 87JDI JDI DEPUY ORTHOPAEDICS, INC. NA UNK

Patients

Seq Age Sex Outcome Treatment
1 77 YR Required Intervention