MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US CORAIL HA W/ COLLAR S12 150MM; OTHER PRODUCTS

Catalog Number L92502

Device Problem Biocompatibility (2886)

Patient Problems Pain (1994); Tissue Damage (2104); Discomfort (2330); Test Result (2695); No Code Available (3191)

Event Date 09/02/2012

Event Type  Injury  

Manufacturer Narrative

Product complaint # (b)(4).If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.(b)(4).Occupation: attorney.

Event Description

Patient was revised bilaterally to address pain.Update 10/29/2012 - litigation papers received.In addition to pain, it is now alleged that the patient.Suffers from discomfort, inflammation, a popping sensation, and metallosis.Doi: (b)(6) 2004 - dor: (b)(6) 2012 (left); doi: (b)(6) 2004 - dor: (b)(6) 2012 (right).Update ad 25 feb 2019: receipt of ppf and implant records.In addition to what were previously alleged, ppf alleges metal wear and elevated metal ions.

Manufacturer Narrative

Depuy synthes is submitting this report pursuant to the provision of 21 cfr, part 803.The report may be based on the information which depuy synthes has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, depuy synthes or its employees that the report constitutes an admission that the device, depuy synthes, or its employees caused or contributed to the potential event described in this report.H10 additional narrative: product complaint #: (b)(4).Investigation summary: no device associated with this report was received for examination.A worldwide complaint database search found no other related reported incidents against the provided product code/lot number combination since release for distribution.Based on previous investigations, this complication of joint replacement is unlikely to have been the result of a device failing to meet required specifications.The information received will be retained for potential series investigations if triggered by trend analysis, post market surveillance, or other events within the quality system.Device history lot: null.Device history batch: null.Device history review: null.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.

• Brand Name: CORAIL HA W/ COLLAR S12 150MM
• Type of Device: OTHER PRODUCTS
• Manufacturer (Section D): DEPUY ORTHOPAEDICS INC US; 700 orthopaedic drive; warsaw IN 46581 0988
• MDR Report Key: 8407733
• MDR Text Key: 138374388
• Report Number: 1818910-2019-86884
• Device Sequence Number: 1
• Product Code: KWL
• Combination Product (y/n): N
• PMA/PMN Number: K123991
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: consumer,other
• Type of Report: Initial,Followup
• Report Date: 02/25/2019

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 03/11/2019
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Expiration Date: 11/02/2009
• Device Catalogue Number: L92502
• Device Lot Number: 1812166
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 10/23/2019
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention
• Patient Age: 66 YR