MAUDE Adverse Event Report: DePuy Ireland - 9616671 ATTUNE; Attune Cementless Implants : Knee Femoral

Catalog Number	150401125
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Muscular Rigidity (1968); Pain (1994)
Date of Event	07/13/2026
Type of Reportable Event	Serious Injury
Event or Problem Description
Subject id: (b)(4).Study no: (b)(6).Clinical adverse event received for revision ¿ pain/stiffness.Device related: no information provided.Procedure related: no information provided.Date of event: (b)(6) 2026.Date of implant: no information provided.Date of revision: (b)(6) 2026.Device location: no information provided.Treatment/impact: revision, depuy synthes components removed (femoral : yes, insert : yes).Depuy synthes products used: date of implant: (b)(6) 2025.Device location: left.Catalog number: 150401125.Lot number id: no information provided.Component type: femoral.Description: attune knee system femoral porocoat cruciate retaining narrow size 5n left cementless.Catalog number: 151820506.Lot number id: m97p28.Component type: insert.Description: attune knee system tibial insert fixed bearing medial stabilized left aox 5, 6mm.
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.D4: udi: as the lot number for the device involved in the event was not provided, the full udi is currently not available.Investigation summary no device associated with this report was received for examination.An evaluation of the manufacturing record could not be performed as the required product/lot number was not provided to complete the evaluation.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 the device lot number is unknown, therefore a¿device history review could not be performed.¿ if the lot/serial number becomes available, the record will be re-assessed.

• Brand Name: ATTUNE
• Common Device Name: Attune Cementless Implants : Knee Femoral
• Manufacturer (Section D): DePuy Ireland - 9616671; loughbeg ringaskiddy co.; cork ; EI
• Manufacturer (Section G): JTE Warsaw Mfg Site; 700 orthopaedic drive; warsaw IN 46582
• Manufacturer Contact: elba bello ; 700 orthopaedic dr.; warsaw, IN 46581 ; +1(908)386-3534
• MDR Report Key: 50224519
• Report Number: 1818910-2026-13801
• Device Sequence Number: 12148939
• Product Code: JWH
• UDI-Device Identifier: 10603295041429
• UDI-Public: (01)10603295041429
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K233980
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2025
• Device Explanted Year: 2026
• Reporter Type: Manufacturer
• Report Source: Study,Health Professional
• Initial Reporter Occupation: Physician
• Type of Report: Initial

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Catalogue Number: 150401125
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Initial Date Received by Manufacturer: 07/20/2026
• Initial Report FDA Received Date: 08/12/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• 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
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 54 YR
• Patient Sex: Female
• Patient Weight: 206 LB