MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US SELF CENT HIP 50X28 BRN; HEMI HIP IMPLANT : HIP ACETABULAR POLY/METAL HEMI

Model Number 1035-50-000

Device Problem Adverse Event Without Identified Device or Use Problem (2993)

Patient Problem Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available (4581)

Event Date 12/27/2020

Event Type  Injury  

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 Description

The patient was revised due to infection.It had nothing whatsoever to do with the implants.The surgeon elected to do a single-stage revision, that included a washout and partial implant swap out.Femoral head and bipolar shell were replaced with the exact same sizes from the primary surgery.There is no other pt info available beyond what's been provided.Doi: (b)(6) 2020, dor: (b)(6) 2020, affected side: left hip.

Manufacturer Narrative

Product complaint # (b)(4).Investigation summary : no device associated with this report was received for examination.The information received will be retained for potential series investigations if triggered by trend analysis or other events within the quality system.Depuy considers the investigation closed.Should additional information be received, the information will be reviewed, and the investigation will be re-opened as necessary.Device history lot : a device history record (mre) review, was not possible because the required lot code was not provided.

• Brand Name: SELF CENT HIP 50X28 BRN
• Type of Device: HEMI HIP IMPLANT : HIP ACETABULAR POLY/METAL HEMI
• Manufacturer (Section D): DEPUY ORTHOPAEDICS INC US; 700 orthopaedic drive; warsaw IN 46581 0988
• MDR Report Key: 11130992
• MDR Text Key: 225515146
• Report Number: 1818910-2021-00574
• Device Sequence Number: 1
• Product Code: KWY
• UDI-Device Identifier: 10603295003403
• UDI-Public: 10603295003403
• Combination Product (y/n): N
• PMA/PMN Number: K812672
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative,health
• Type of Report: Initial,Followup
• Report Date: 12/27/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 01/07/2021
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Model Number: 1035-50-000
• Device Catalogue Number: 103550000
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 02/09/2021
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Treatment: ARTICULEZE M 28MM 5; SELF CENT HIP 50X28 BRN; ARTICULEZE M 28MM 5; SELF CENT HIP 50X28 BRN
• Patient Outcome(s): Required Intervention
• Patient Age: 82 YR