MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US DUR DYNAMIC LOCK RING 60 OR 72; DURALOC IMPLANT : HIP ACETABULAR AUGMENT

Catalog Number	124960000
Medical Device Problem Code	Insufficient Device Problem Information (3190)
Health Effect - Clinical Codes	Hematoma (1884); Pain (1994); Not Applicable (3189)
Date of Event	03/05/2018
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
(b)(4).If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Event or Problem Description
Patient was revised to address pain and suspected metallosis from cables or stem trunnion.Surgeon found no signs of metallosis but found a large hematoma.Surgeon cleaned out the wound and replaced the head (competitor), liner and locking ring.Doi: unknown; dor: (b)(6) ,2018; right hip.
Additional Manufacturer Narrative
Product complaint # = > pc-(b)(4).Corrected lot number.
Additional Manufacturer Narrative
Product complaint # : (b)(4).No device associated with this report was received for examination.A worldwide complaint database search found no other reported incident(s) against the provided product/lot combination(s) since release for distribution.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate. .

• Brand Name: DUR DYNAMIC LOCK RING 60 OR 72
• Common Device Name: DURALOC IMPLANT : HIP ACETABULAR AUGMENT
• Manufacturer (Section D): DEPUY ORTHOPAEDICS INC US; 700 orthopaedic drive; warsaw IN 46582 0988
• MDR Report Key: 7377123
• Report Number: 1818910-2018-56266
• Device Sequence Number: 13814508
• Product Code: LZO
• UDI-Device Identifier: 10603295019800
• UDI-Public: 10603295019800
• Combination Product (Y/N): N
• Initial Reporter State: OR
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Explanted Year: 2018
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Health Professional
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 03/05/2018

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Catalogue Number: 124960000
• Device Lot Number: S51DT1006
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 03/05/2018
• Supplement Date Received by Manufacturer: 03/05/2018; 04/11/2018
• Initial Report FDA Received Date: 03/28/2018
• Supplement Report FDA Received Date: 03/28/2018; 04/13/2018
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 73 YR