MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US PROTRUSIO CAGE 52OD X 49ID L; MISCELLANEOUS JOINT IMPLANTS : HIP ACETABULAR CAGES

Model Number 1011-72-000

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

Patient Problems Adhesion(s) (1695); Unspecified Infection (1930); Scar Tissue (2060)

Event Date 08/06/2009

Event Type  Injury  

Manufacturer Narrative

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

Event Description

Pc was created to capture the event.(pg 2560) on (b)(6) 2009 operative records indicate the patient received a left total hip revision due to significant scarring and gross infection.Acetabular cage and prostalac was removed and irrigation and debridement was performed.Doi: (b)(6) 2009.Dor: (b)(6) 2009.Left hip.

Manufacturer Narrative

Product complaint # (b)(4).Investigation summary : no device associated with this report was received for examination.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.Depuy considers the investigation closed.Should additional information be received, the information will be reviewed and the investigation will be re-opened as necessary.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.

• Brand Name: PROTRUSIO CAGE 52OD X 49ID L
• Type of Device: MISCELLANEOUS JOINT IMPLANTS : HIP ACETABULAR CAGES
• Manufacturer (Section D): DEPUY ORTHOPAEDICS INC US; 700 orthopaedic drive; warsaw IN 46581 0988
• 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: 14732251
• MDR Text Key: 294837789
• Report Number: 1818910-2022-11109
• Device Sequence Number: 1
• Product Code: JDJ
• UDI-Device Identifier: 10603295000549
• UDI-Public: 10603295000549
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K962007
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Other
• Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date: 06/17/2022

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 06/17/2022
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Expiration Date: 01/31/2010
• Device Model Number: 1011-72-000
• Device Catalogue Number: 101172000
• Device Lot Number: UC8F21029
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Date Manufacturer Received: 06/20/2022
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 01/26/2000
• 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
• Patient Outcome(s): Required Intervention
• Patient Age: 54 YR
• Patient Sex: Female