MAUDE Adverse Event Report: DEPUY IRELAND - 9616671 UNK KNEE TIBIAL INSERT ATTUNE REVISION

Catalog Number UNK KNEE TIBIAL INSERT ATTUNE

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

Patient Problem Unspecified Infection (1930)

Event Date 08/23/2022

Event Type  Injury  

Event Description

Patient was revised due to mrsa infection.The implants were removed and antibiotics and temporary implants were inserted.The patient was from (b)(6) and the prior surgery was done in 2018.There was no surgical delay.Doi: (b)(6) 2018, dor: (b)(6) 2022, affected side: left knee.

Manufacturer Narrative

Product complaint # (b)(4).The device catalog number is unknown; therefore, udi is unavailable.Depuy synthes is submitting this report pursuant to the provisions of 21 cfr, part 803.This report may be based on information which depuy synthes has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, depuy synthes or its employees that the report constitutes an admission that the device, depuy synthes, or its employees caused or contributed to the potential event described in this report.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.

Manufacturer Narrative

Product complaint # (b)(4).Investigation summary: no device associated with this report was received for examination.A worldwide lot specific complaint database search, or manufacturing record evaluation, was not possible as the required lot number was not provided.The information received will be retained for trend analysis, post market surveillance, or other events within the quality system.Device history lot: a manufacturing record evaluation (mre), was not possible because the required lot code was not provided.This medwatch report was initially submitted on 9/23/2022.This report is being resubmitted as this report failed submission as a result of the electronic gateway.Please reference fda ticket (b)(4) for additional details.

• Brand Name: UNK KNEE TIBIAL INSERT ATTUNE REVISION
• Type of Device: KNEE TIBIAL INSERT
• Manufacturer (Section D): DEPUY IRELAND - 9616671; loughbeg ringaskiddy co.; cork ; EI
• Manufacturer (Section G): DEPUY ORTHOPAEDICS, INC. 1818910; 700 orthopaedic dr.; warsaw IN 46581 0988
• Manufacturer Contact: kate karberg ; 700 orthpaedic dr.; warsaw, IN 46581 ; 3035526892
• MDR Report Key: 15371205
• MDR Text Key: 299386168
• Report Number: 1818910-2022-17316
• Device Sequence Number: 1
• Product Code: LPH
• Combination Product (y/n): N
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Health Professional,Company Representative
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date: 09/23/2022

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 09/07/2022
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Catalogue Number: UNK KNEE TIBIAL INSERT ATTUNE
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 09/22/2022
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Treatment: ATTUNE DISTAL AUGMENTS .4MM; ATTUNE DISTAL AUGMENTS .4MM; ATTUNE FEMORAL SLEEVE SZ40; ATTUNE POSTERIOR AUGMENT 4MM; ATTUNE POSTERIOR AUGMENT 8MM; ATTUNE PRESS FIT STEM 14X110; ATTUNE PRESS FIT STEM 18X60; ATTUNE REV FEMUR SZ 9 LEFT; ATTUNE RP REVISION TIBIA SZ 9; ATTUNE TIBIA SLEEVE SZ 37; ATTUNE TIBIA SLEEVE SZ 37; BONE CEMENT (MFG. AND PRODUCT NAME UNKNOWN)
• Patient Outcome(s): Required Intervention
• Patient Age: 72 YR
• Patient Sex: Male