MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US PINNACLE MTL INS NEUT36IDX54OD; PINNACLE HIP SYSTEM : HIP METAL ACETABULAR LINERS

Model Number 1218-87-354

Device Problem Adverse Event Without Identified Device or Use Problem (2993)

Patient Problems Adhesion(s) (1695); Foreign Body Reaction (1868); Hypersensitivity/Allergic reaction (1907); Unspecified Infection (1930); Scarring (2061); No Code Available (3191)

Event Date 05/07/2020

Event Type  Injury  

Manufacturer Narrative

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

Event Description

The primary surgery was performed on (b)(6) 2010 via tha for the patient¿s right hip joint.It was reported that the revision surgery was performed on (b)(6) 2020 by replacing the liner (p/n: 121887354), the head (p/n: 962713000) and the stem (p/n: 900534210) due to suspicion of infection.Before the surgery, the pseudotumor was not found by x-rays, and the surgeon had a difficulty in judging whether there was infection although there was rising crp level.There was no anathema and redness around the primary surgery¿s incision.During the revision surgery, the surgeon found that the head and the neck-junction of the stem were black discolored and surrounding tissue was covered with scarring tissue.The revision surgery was completed, and it was unknown whether there was any surgical delay.The surgeon commented that this result was as per reported mom case, and it was expected result in consideration of the patient¿s high activity, sex (male) and mom.No further information is available.

Manufacturer 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 reported incident(s) against the provided product/lot combination(s) 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.Corrective action was not indicated.

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.H6 patient code: no code available (3191) is used to capture device revision or replacement.If information is obtained that was not available for the initial report, a follow-up report will be filed as appropriate.

• Brand Name: PINNACLE MTL INS NEUT36IDX54OD
• Type of Device: PINNACLE HIP SYSTEM : HIP METAL ACETABULAR LINERS
• Manufacturer (Section D): DEPUY ORTHOPAEDICS INC US; 700 orthopaedic drive; warsaw IN 46581 0988
• MDR Report Key: 10075005
• MDR Text Key: 191565389
• Report Number: 1818910-2020-12338
• Device Sequence Number: 1
• Product Code: KWA
• Combination Product (y/n): N
• PMA/PMN Number: K003523
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: foreign,health professional,o
• Type of Report: Initial,Followup,Followup
• Report Date: 05/06/2020

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
• Device Operator: Health Professional
• Device Model Number: 1218-87-354
• Device Catalogue Number: 121887354
• Device Lot Number: 3098031
• Was Device Available for Evaluation?: No
• Initial Date Manufacturer Received: 05/06/2020
• Initial Date FDA Received: 05/20/2020
• Supplement Dates Manufacturer Received: 06/04/2020; 06/23/2020
• Supplement Dates FDA Received: 06/08/2020; 06/24/2020
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Treatment: 9/10 ULTAMET 36MM HEADS +6; PINNACLE-A SCREW 6.5X15; PINNACLE-A SCREW 6.5X30; S-ROM*SLEEVE PRX ZTT, 18F-LRG; 9/10 ULTAMET 36MM HEADS +6; PINNACLE-A SCREW 6.5X15; PINNACLE-A SCREW 6.5X30; S-ROM*SLEEVE PRX ZTT, 18F-LRG
• Patient Outcome(s): Required Intervention
• Patient Age: 56 YR