MAUDE Adverse Event Report: DEPUY JOHNSON AND JOHNSON DEPUY HIP

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

Patient Problem Disability (2371)

Event Date 06/05/2012

Event Type  Injury  

Event Description

Johnson and johnson metal on metal hip.I was disabled over it.And i've had lawyers on it since 2013 to no avail.

• Brand Name: JOHNSON AND JOHNSON DEPUY HIP
• Type of Device: JOHNSON AND JOHNSON
• Manufacturer (Section D): DEPUY
• MDR Report Key: 7214973
• MDR Text Key: 98223139
• Report Number: MW5074775
• Device Sequence Number: 1
• Product Code: LZO
• Combination Product (y/n): N
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Voluntary
• Reporter Occupation: Patient
• Type of Report: Initial
• Report Date: 01/10/2018

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
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Initial Date Manufacturer Received: Not provided
• Initial Date FDA Received: 01/23/2018
• Was Device Evaluated by Manufacturer?: No Information
• Is This a Reprocessed and Reused Single-Use Device?: Yes
• Type of Device Usage: N
• Patient Sequence Number: 1
• Patient Outcome(s): Disability
• Patient Age: 52 YR
• Patient Weight: 82