FDA Adverse Event Injury Summary report: N

TOTAL HIP BALL 28MM +5

MDR report key: 1222438 · Received November 4, 2008

Report

Report Number
1818910-2008-05128
Event Type
Injury
Date Received
November 4, 2008
Date of Event
October 23, 2008
Report Date
October 23, 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
SD, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

EXAMINATION WAS NOT POSSIBLE, AS THE DEVICES WERE NOT RETURNED. A COMPLAINT DATABASE SEARCH FINDS NO OTHER REPORTED INCIDENTS AGAINST THE PROVIDED PRODUCT AND LOT CODES SINCE THEIR RELEASE FOR DISTRIBUTION. THE INVESTIGATION COULD NOT VERIFY OR IDENTIFY ANY EVIDENCE OF PRODUCT ERROR WITH REGARD TO THE REPORTED EVENT. BASED ON THE INVESTIGATION, THE NEED FOR CORRECTIVE ACTION IS NOT INDICATED.

Description of Event or Problem · 1

PT WAS REVISED TO ADDRESS CHRONIC DISLOCATION (RIGHT SIDE).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTAL HIP BALL 28MM +5 87JDI JDI DEPUY ORTHOPAEDICS, INC. NA 922800012

Patients

Seq Age Sex Outcome Treatment
1 78 YR Required Intervention