inforMED
InjuryHTG

UNKNOWN DEPUY PATELLA

Received Feb 6, 2012 · Event occurred Jan 9, 2012

Report 1818910-2012-02816 · MDR key 2439579

Device

Generic name

Patella

Manufacturer

Depuy Warsaw

Catalog number

UNKNOWN

Lot number

UNKNOWN

Product problems

  • Insufficient Device Problem Information

Patient

43 YR

  • Unspecified Infection

Narrative

Description of Event or Problem

PATIENT WAS REVISED FOR POSSIBLE INFECTION AND MINIMAL OSTEOLYSIS.

Additional Manufacturer Narrative

THIS COMPLAINT IS STILL UNDER INVESTIGATION. DEPUY WILL NOTIFY THE FDA OF THE RESULTS OF THIS INVESTIGATION ONCE IT HAS BEEN COMPLETED.

Additional Manufacturer Narrative

THE PRODUCT ASSOCIATED WITH THIS REPORTED EVENT WAS NOT RETURNED FOR EXAMINATION. THE PRODUCT CODE AND LOT CODE REQUIRED IN RETRIEVING THE DEVICE HISTORY RECORDS FOR REVIEWING AND SEARCHING THE COMPLAINT DATABASE WERE NOT PROVIDED. THE INVESTIGATION COULD NOT DRAW ANY CONCLUSIONS ABOUT THE REPORTED INFECTION BASED ON THE PROVIDED INFORMATION. BASED ON THE PERFORMED INVESTIGATION, THE NEED FOR CORRECTIVE ACTION IS NOT INDICATED. DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD ADDITIONAL INFORMATION BE RECEIVED, THE INVESTIGATION WILL BE RE-OPENED.

Remedial action

  • Other