FDA Adverse Event Injury Summary report: N

PINNACLE MTL INS NEUT36IDX58OD

MDR report key: 3417003 · Received October 17, 2013

Report

Report Number
1818910-2013-30853
Event Type
Injury
Date Received
October 17, 2013
Date of Event
October 10, 2013
Report Date
October 14, 2013
Manufacturer
DEPUY ORTHOPAEDICS, INC. 1818910 
Product Code
KWA
PMA / PMN Number
PK003523
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
ATTORNEY

Narratives

Additional Manufacturer Narrative · 1

UPDATE: THE DEVICES ASSOCIATED WITH THIS REPORT WERE NOT RETURNED. A PREVIOUS REVIEW OF THE DEVICE HISTORY RECORDS FOR LOT CODES 1803019 AND 1823078 DID NOT REVEAL ANY RELATED MANUFACTURING ANOMALIES. THE INVESTIGATION COULD NOT VERIFY OR IDENTIFY ANY PRODUCT CONTRIBUTION TO THE REPORTED EVENT WITH THE INFORMATION PROVIDED. BASED ON THE INABILITY TO DETERMINE A ROOT CAUSE, THE NEED FOR CORRECTIVE ACTION WAS NOT INDICATED. DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD ADDITIONAL INFORMATION BE RECEIVED, THE INFORMATION WILL BE REVIEWED AND THE INVESTIGATION WILL BE RE-OPENED AS NECESSARY.

Additional Manufacturer Narrative · 1

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

Additional Manufacturer Narrative · 1

(B)(4).

Description of Event or Problem · 1

LITIGATION ALLEGES THAT THE PATIENT SUFFERS FROM PAIN, DISCOMFORT, INFLAMMATION, AND LARGE AMOUNTS OF TOXIC COBALT CHROMIUM METAL ION PARTICLES TO BE RELEASED INTO THE BLOOD, TISSUE, AND BONE.

Description of Event or Problem · 1

ADDED STEM ON IP DUE TO PREVIOUSLY ALLEGED LARGE AMOUNTS OF TOXIC COBALT CHROMIUM METAL IONS, LAWYER AND LAW FIRM. UPDATED DOI.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
532278 PINNACLE MTL INS NEUT36IDX58OD PINNACLE HIP SYSTEM : HIP METAL ACETABULAR LINERS KWA DEPUY ORTHOPAEDICS, INC. 1818910  1803019

Patients

Seq Age Sex Outcome Treatment
1 Other