MAUDE Adverse Event Report: DEPUY IRELAND - 9616671 12/14 ARTICUL 40MM TRIAL +8.5; FEMORAL TRIALS

Catalog Number 253107000

Device Problems Naturally Worn (2988); Scratched Material (3020)

Patient Problem No Clinical Signs, Symptoms or Conditions (4582)

Event Date 01/01/2023

Event Type  malfunction  

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

Complaint is related to (b)(4).This complaint was created due to the excess impacted products in (b)(4).Damaged plastic femoral head trials - need replacement.Plastic is worn and scratched on head trials.

Event Description

Additional information received: a.What was specifically the damage on the devices (broken (2+ pieces), cracked, bent, stripped/worn).Plastic is worn and scratched on head trials b.Can you please provide the lot no of the reported products? working with ops to swap out, lot numbers will.Be available on return of trial heads c.What is the event date? as reported by the pc- heads have been worn over time with use d.Were there any adverse consequence/s that affected the patient because of the reported event? no.E.Did the event occur during the surgery? if yes, was there a surgical delay? what is the duration of the delay? no, identified outside surgery.

Manufacturer Narrative

Product complaint # (b)(4).Investigation summary according to the information received, "damaged plastic femoral head trials - need replacement" the product was not returned to depuy synthes, however photos were provided for review.The photographs attached were reviewed, however they do not represent the reported complaint condition.Therefore, the investigation could not draw any conclusions about the reported event due to the insufficient evidence provided.The overall complaint was unconfirmed as the photographs provided are not representative of the reported complaint condition.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 complaint condition.As part of depuy synthes 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 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.H10 additional narrative:.

• Brand Name: 12/14 ARTICUL 40MM TRIAL +8.5
• Type of Device: FEMORAL TRIALS
• Manufacturer (Section D): DEPUY IRELAND - 9616671; loughbeg ringaskiddy co.; cork ; EI
• Manufacturer (Section G): DEPUY ORTHOPAEDICS, INC. 1818910; 700 orthopaedic dr.; warsaw IN 46581 0988
• Manufacturer Contact: kate karberg ; 700 orthopaedic dr.; warsaw, IN 46581-0988 ; 3035526892
• MDR Report Key: 18434844
• MDR Text Key: 331913262
• Report Number: 1818910-2024-00190
• Device Sequence Number: 1
• Product Code: HWT
• UDI-Device Identifier: 10603295129073
• UDI-Public: 10603295129073
• Combination Product (y/n): N
• Reporter Country Code: AS
• PMA/PMN Number: EXEMPT
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Foreign,Health Professional,Company Representative
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date: 01/03/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 01/03/2024
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Catalogue Number: 253107000
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 02/12/2024
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Unknown
• Patient Sequence Number: 1