MAUDE Adverse Event Report: DEPUY IRELAND 9616671 ATTUNE CR FEM RT SZ 5 NAR CEM; ATTUNE IMPLANT : KNEE FEMORAL

Catalog Number 150400225

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

Patient Problems Pain (1994); No Code Available (3191)

Event Date 05/10/2016

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 had a valgus knee.The surgeon used the prescribed technique using a measured sizer.A size 5 narrow femur, size 6 tibia tray and as sz 5 8mm poly were implanted.The patient was balanced in both extension and flexion with the 8mm poly.3 days later the patient was experiencing some pain, an x-ray was taken which showed that the insert had spun out.The surgeon did an mua and then subsequently decided to change the poly.On manipulation in theater it was quite obvious that the knee was very unstable.The 8mm poly was removed and a sz5 14mm poly insert was implanted.

Manufacturer Narrative

Product complaint # (b)(4).No device associated with this report was received for examination.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.

• Brand Name: ATTUNE CR FEM RT SZ 5 NAR CEM
• Type of Device: ATTUNE IMPLANT : KNEE FEMORAL
• Manufacturer (Section D): DEPUY IRELAND 9616671; loughbeg, ringaskiddy co.; cork ; EI
• MDR Report Key: 8223169
• MDR Text Key: 132260507
• Report Number: 1818910-2019-80056
• Device Sequence Number: 1
• Product Code: JWH
• UDI-Device Identifier: 10603295041283
• UDI-Public: 10603295041283
• Combination Product (y/n): N
• PMA/PMN Number: K101433
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: foreign,health professional,o
• Type of Report: Initial,Followup
• Report Date: 12/10/2018

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 01/07/2019
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Catalogue Number: 150400225
• Device Lot Number: 8226982
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 02/05/2019
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention