MAUDE Adverse Event Report: DEPUY IRELAND - 9616671 ATTUNE PS FEM RT SZ 8 CEM; ATTUNE IMPLANT : KNEE FEMORAL

Model Number	1504-10-208
Medical Device Problem Codes	Tear, Rip or Hole in Device Packaging (2385); Device Contaminated During Manufacture or Shipping (2969)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	02/27/2023
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Product complaint #: (b)(4).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.
Event or Problem Description
It was reported that the seal of the sterile container was broken before given to nurse so implant is not able to be used.There was no surgical delay.Affected side: right knee.
Additional Manufacturer Narrative
Product complaint # (b)(4).This report is being submitted pursuant to the provisions of 21 cfr, part 803.This report may be based on information which has not been investigated or verified prior to the required reporting date.This report does not reflect a conclusion by depuy synthes joint reconstruction, or its employees that the report constitutes an admission that the product, depuy synthes joint reconstruction, 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 report, a follow-up report will be filed as appropriate.
Additional Manufacturer Narrative
Product complaint # (b)(4).Investigation summary: the product was returned to depuy synthes for evaluation.The depuy synthes team forwarded the device to depuy cork which conducted a visual inspection of the returned device.On examination of the returned complaint unit, it was observed that there was damaged on the tab in the inner blister, however the tyvek seal was no breached.There is no impact on the sterility of the unit or integrity of the sterile barrier.However the current complaint condition cannot be attributed to a manufacturing issue.Additional monitoring for any potential safety signals will be conducted through complaint trending and other post-market safety surveillance activities.Device history lot: 1) quantity manufactured: 12 parts were manufactured to specification.2) date of manufacture: 02/03/2022.3) any anomalies or deviations identified in dhr: 7 non-conformances associated with this lot.There is no potential correlation between this non-conformance and the failure mode of the complaint.4) expiry date: 01/31/2032.5) ifu reference: ifu-0902-00-828.Device history review: 1) quantity manufactured: 12 parts were manufactured to specification.2) date of manufacture: 02/03/2022.3) any anomalies or deviations identified in dhr: 7 non-conformances associated with this lot.There is no potential correlation between this non-conformance and the failure mode of the complaint.4) expiry date: 01/31/2032.5) ifu reference: ifu-0902-00-828.

• Brand Name: ATTUNE PS FEM RT SZ 8 CEM
• Common Device Name: ATTUNE IMPLANT : KNEE FEMORAL
• Manufacturer (Section D): DEPUY IRELAND - 9616671; loughbeg ringaskiddy co.; cork ; EI
• Manufacturer (Section G): DEPUY IRELAND 9616671; loughbeg, ringaskiddy co.; cork ; EI
• Manufacturer Contact: kate karberg ; 700 orthpaedic dr.; warsaw, IN 46581 ; 3035526892
• MDR Report Key: 16521950
• Report Number: 1818910-2023-05555
• Device Sequence Number: 11366495
• Product Code: JWH
• UDI-Device Identifier: 10603295041795
• UDI-Public: 10603295041795
• Combination Product (Y/N): N
• Initial Reporter State: GA
• Initial Reporter Country: US
• PMA/510(K) Number: P830055
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 03/10/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: 1504-10-208
• Device Catalogue Number: 150410208
• Device Lot Number: 3679203
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 02/27/2023
• Supplement Date Received by Manufacturer: 03/16/2023; 09/07/2023
• Initial Report FDA Received Date: 03/10/2023
• Supplement Report FDA Received Date: 03/17/2023; 09/08/2023
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 02/03/2022
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown