MAUDE Adverse Event Report: OMNILIFE SCIENCE, INC. OMNI HIP SYSTEM; PROSTHESIS, HIP, SEMI-CONSTRAINED

Catalog Number	HC-21003-HA
Health Effect - Clinical Code	Pain (1994)
Date of Event	08/08/2018
Type of Reportable Event	Serious Injury
Event or Problem Description
The complaint involved a patient who underwent hip revision surgery on (b)(6) 2018.The original surgery is dated (b)(6) 2013.The revision surgery occured because of reported patient pain.During the revision, the omni arc stem, modular neck and ceramic femoral head were removed and replaced with non-omni components.

• Brand Name: OMNI HIP SYSTEM
• Common Device Name: PROSTHESIS, HIP, SEMI-CONSTRAINED
• Manufacturer (Section D): OMNILIFE SCIENCE, INC.; 480 paramount drive; raynham MA 02767
• MDR Report Key: 7986399
• Report Number: 1226188-2018-00125
• Device Sequence Number: 1572285
• Product Code: LPH
• UDI-Device Identifier: 00841690115816
• UDI-Public: 00841690115816
• Combination Product (Y/N): N
• PMA/510(K) Number: K090845
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2013
• Device Explanted Year: 2018
• Reporter Type: Manufacturer
• Report Source: company representative
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 08/09/2018

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?: No
• Operator of Device: Health Professional
• Device Expiration Date: 05/31/2017
• Device Catalogue Number: HC-21003-HA
• Device Lot Number: 11611
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 08/09/2018
• Initial Report FDA Received Date: 10/19/2018
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Hospitalization; Required Intervention
• Patient Age: 65 YR