MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US TOTAL HIP BALL 28MM +8; LARGE TAPER FEMORAL HEADS : HIP METAL FEMORAL HEADS

Catalog Number 101814000

Device Problem Naturally Worn (2988)

Patient Problem Insufficient Information (4580)

Event Date 01/04/2024

Event Type  Injury  

Event Description

Patient was revised due to the cup that dislocated.Doi: unknown.Dor: (b)(4) 2024.Affected side: unknown.

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 report, a follow-up report will be filed as appropriate.

Event Description

The patient had a depuy cup/liner/head/stem.The cup and liner were noted to be "extremely worn".There was no dislocation or disassociation, the sales rep said that the liner was "gone" due to wear.The acetabular cup/liner/and head were removed.The acetabular side was replaced with competitor products, while a depuy femoral head was implanted on the femoral side.The stem remained in-situ.There was no allegation of deficiency for the femoral head that was revised.

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.

Manufacturer Narrative

Product complaint # (b)(4).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 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 lot : 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: TOTAL HIP BALL 28MM +8
• Type of Device: LARGE TAPER FEMORAL HEADS : HIP METAL FEMORAL HEADS
• 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
• Manufacturer Contact: kate karberg ; 700 orthopaedic dr.; warsaw, IN 46581-0988 ; 3035526892
• MDR Report Key: 18501835
• MDR Text Key: 332761419
• Report Number: 1818910-2024-00927
• Device Sequence Number: 1
• Product Code: JDI
• UDI-Device Identifier: 10603295001355
• UDI-Public: 10603295001355
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K860701
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Health Professional,Company Representative
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup,Followup
• Report Date: 01/12/2024

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?: Yes
• Device Operator: Health Professional
• Device Catalogue Number: 101814000
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Initial Date Manufacturer Received: 01/04/2024
• Initial Date FDA Received: 01/12/2024
• Supplement Dates Manufacturer Received: 01/19/2024; 01/24/2024
• Supplement Dates FDA Received: 01/22/2024; 01/29/2024
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Treatment: UNK HIP ACETABULAR CUP AML.; UNK HIP ACETABULAR LINER POLY AML.
• Patient Outcome(s): Required Intervention
• Patient Sex: Male