MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US PINNACLE SECTOR II CUP 58MM; PINNACLE HIP SYSTEM : HIP METAL ACETABULAR CUPS

Catalog Number	121722058
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Pain (1994); Loss of Range of Motion (2032); Numbness (2415); Joint Laxity (4526)
Date of Event	06/18/2021
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Product complaint # (b)(4).Investigation summary: no device associated with this report was received for examination.The product investigation found no evidence suspecting an error in the manufacturing or material that would be a contributing factor in the reported allegation(s).A records evaluation (mre) was not perform.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: the product investigation found no evidence suspecting an error in the manufacturing or material that would be a contributing factor in the reported allegation(s).A manufacturing records evaluation (mre) was not performed.
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.H10 additional narrative: added: a2, b7 if information is obtained that was not available for the initial report, a follow-up report will be filed as appropriate.
Event or Problem Description
Litigation records ad 3&4 aug 2023 alleges on june 18, 2021, the depuy corail® stem at the neck on the patient's right hip, without warning, suddenly and catastrophically fractured at the neck while patient was simply walking.Patient suffered significant damages including, but not limited to physical injury, economic loss, pain and suffering, and will continue to suffer damages into the foreseeable future.Doi: (b)(6) 2011.Doe: jun 18, 2021.Dor: (b)(6) 2021.Affected side: right hip.This pc was re-opened due to additional information received from (b)(6) on 3 jul 2024.
Additional Manufacturer Narrative
Product complaint # (b)(4).E3 initial reporter occupation: lawyer.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 report, a follow-up report will be filed as appropriate.
Event or Problem Description
Medical records received.On (b)(6) 2014, the patient underwent a right hip arthroscopy with labral repair, fractional lengthening of the iliopsoas tendon and extensive debridement and synovectomy due to a right hip snapping iliopsoas tendon due to impingement syndrome.The right hip implant was noted to be well-fixed and stable.On (b)(6) 2011 patient had a right total hip arthroplasty.(no specifics provided in this set of medical records).(b)(6) 2014 medical records note the patient underwent a right hip arthroplasty approximately three years ago.The patient has noticed more pain, limited mobility, numbness or tingling down right lateral aspect of the leg.Radiographs noted narrowing of the l5-s1 disc space with foraminal stenosis.On (b)(6) 2014 medical records note the patient is having follow-up after getting a right hip iliopsoas injection.Patient shows pain and mild crepitus.On (b)(6) 2014, the patient had a right hip arthroscopy with anterior labral repair and osteoplasty of the femoral neck and acetabulum with labral debridement and chondroplasty, with extensive synovectomy to address right hip femoroacetabular impingement with anterior labral tear.
Additional Manufacturer Narrative
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: litigation records ad 3&4 aug 2023 alleges on (b)(6) 2021, the depuy corail® stem at the neck on the patient's right hip, without warning, suddenly and catastrophically fractured at the neck while patient was simply walking.Patient suffered significant damages including, but not limited to physical injury, economic loss, pain and suffering, and will continue to suffer damages into the foreseeable future.The product was not returned to j&j medtech orthopaedics; however, photos were provided for review.See attachment (b)(4); x-rays from disc.The x-ray investigation revealed nothing indicative of a device nonconformance.A manufacturing record evaluation was performed for the finished device product code: 121722058 lot number: ff7jt1, and no non-conformances or manufacturing irregularities related to the reported complaint condition were identified.As the device was not returned, an as-received condition could not be assessed, and a dimensional inspection and document/specification review were not completed.The overall complaint was not confirmed as the observed condition of the pinnacle sector ii cup 58mm would not have contributed to the reported adverse event.Based on the investigation findings, it has been determined that no corrective and/or preventative action is proposed.There is no indication that a design or manufacturing issue has caused the reported complaint condition.As part of j&j medtech orthopaedics quality process, all devices are manufactured, inspected, and released to approved specifications.Additional monitoring for any potential safety signals will be conducted through complaint trending and other post-market safety surveillance activities.Device history lot: a manufacturing record evaluation was performed for the finished device product code: 121722058 lot number: ff7jt1, and no non-conformances or manufacturing irregularities related to the reported complaint condition were identified.
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 hat 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.H11 additional narrative: added: b6 and b7.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).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.H11 additional narrative: added: b7.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).This report is being submitted pursuant to the provisions of 21 cfr, part 803.This report may be based on information that 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.H11 additional narrative: added : b7.If information that was not available for the initial report is obtained, a follow-up report will be filed as appropriate.

• Brand Name: PINNACLE SECTOR II CUP 58MM
• Common Device Name: PINNACLE HIP SYSTEM : HIP METAL ACETABULAR CUPS
• Manufacturer (Section D): DEPUY ORTHOPAEDICS INC US; 700 orthopaedic drive; warsaw IN 46581 0988
• Manufacturer (Section G): JTE WARSAW MFG SITE; 700 orthopaedic drive; warsaw IN 46582
• Manufacturer Contact: kate karberg ; 700 orthopaedic dr.; warsaw, IN 46581-0988 ; 3035526892
• MDR Report Key: 19712674
• Report Number: 1818910-2024-14966
• Device Sequence Number: 12896960
• Product Code: LPH
• UDI-Device Identifier: 10603295009856
• UDI-Public: (01)10603295009856(10)FF7JT1(17)210218
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: P070026
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2011
• Device Explanted Year: 2021
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Other,Consumer
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup,Followup,Followup,Followup
• Report Date (Section B): 07/10/2024

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 Expiration Date: 02/18/2021
• Device Catalogue Number: 121722058
• Device Lot Number: FF7JT1
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/03/2024
• Supplement Date Received by Manufacturer: 07/18/2024; 07/22/2024; 09/24/2024; 07/23/2025; 09/22/2025; 09/23/2025; 10/13/2025
• Initial Report FDA Received Date: 07/10/2024
• Supplement Report FDA Received Date: 07/18/2024; 07/30/2024; 10/10/2024; 07/24/2025; 09/24/2025; 09/29/2025; 10/16/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 02/21/2011
• 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
• Concomitant Medical Products and Therapy/Usage Dates: ALTRX NEUT 36ID X 58OD.; APEX HOLE ELIM POSITIVE STOP.; ARTICULEZE M HEAD 36 MM +1.5.; CORAIL AMT COLLAR SIZE 13.; PINN CAN BONE SCREW 6.5 MM X 30 MM.
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 63 YR
• Patient Sex: Male