MAUDE Adverse Event Report: DEPUY IRELAND - 9616671 ATTUNE FEM POR CR LT SZ 5; ATTUNE CEMENTLESS IMPLANTS : KNEE FEMORAL

Catalog Number	150401105
Medical Device Problem Code	Difficult to Insert (1316)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	08/25/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Product complaint # (b)(4).This report is being submitted pursuant to the provisions of 21 cfr, part 803 (and/or part 4, as applicable).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, or its employees that the report constitutes an admission that the product, 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 attune cementless femur (porocoat) was very grippy, requires large amount of force to impact it in to seat on the resected bony surface.There was a concern about microfractures given the strong impaction required.There was no patient consequence.
Additional Manufacturer Narrative
Product complaint #(b)(4).Investigation summary: an analysis of the product could not be performed since a physical sample was not received for evaluation.As part of our company quality system process, all devices are manufactured, inspected, and distributed to approved specifications.Based on the information available, there is no indication that a design or manufacturing issue has caused the reported complaint condition, therefore it has been determined that no corrective and preventive action is required at this time.Additional complaint information monitoring for potential safety signals will be conducted through complaint trending as part of the post-market surveillance.However, if the product is received at a later date, the investigation will be updated as applicable.
Additional Manufacturer Narrative
Product complaint # (b)(4).Investigation summary: no device associated with this report was received for examination.According to the information received, ¿attune cementless femur (porocoat) was very grippy, requires large amount of force to impact it in to seat on the resected bony surface.Concerned about microfractures given the strong impaction required.¿ product description:- attune fem por cr lt sz 5, product code:- 150401105, lot no:- 4834692, quantity of manufactured:- 12, date of manufacturing:- 15-jun-2025, expiry date:- 31-may-2035.As part of our company quality system process, all devices are manufactured, inspected, and distributed to approved specifications.Additional complaint information monitoring for potential safety signals will be conducted through complaint trending as part of the post-market surveillance.If additional information is made available, the investigation will be updated as applicable.Device history lot: product description:- attune fem por cr lt sz 5 product code:- 150401105.Lot no:- 4834692.Quantity of manufactured:- 12.Date of manufacturing:- 15-jun-2025.Expiry date:- 31-may-2035.Device history batch: null.Device history review: a manufacturing record evaluation was performed for the finished device [lot no: 4834692 ; part no:150401105] number, and no non-conformances / manufacturing irregularities were identified.H11 additional narrative: corrected: h4.

• Brand Name: ATTUNE FEM POR CR LT SZ 5
• Common Device Name: ATTUNE CEMENTLESS IMPLANTS : KNEE FEMORAL
• Manufacturer (Section D): DEPUY IRELAND - 9616671; loughbeg ringaskiddy co.; cork ; EI
• Manufacturer (Section G): CORK MFG & MATERIAL WAREHOUSE; loughbeg ringaskiddy; cork ; EI
• Manufacturer Contact: elba bello ; 700 orthpaedic dr.; warsaw, IN 46581 ; 9083863534
• MDR Report Key: 23062784
• Report Number: 1818910-2025-15939
• Device Sequence Number: 13228111
• Product Code: MBH
• UDI-Device Identifier: 10603295041344
• UDI-Public: (01)10603295041344(17)350531(10)4834692
• Combination Product (Y/N): N
• Initial Reporter Country: SN
• PMA/510(K) Number: P830055
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2025
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup,Followup

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 Catalogue Number: 150401105
• Device Lot Number: 4834692
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 08/25/2025
• Supplement Date Received by Manufacturer: 09/25/2025; 11/14/2025
• Initial Report FDA Received Date: 09/16/2025
• Supplement Report FDA Received Date: 09/25/2025; 11/14/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 06/15/2025
• 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