MAUDE Adverse Event Report: OMNILIFE SCIENCE, INC. APEX KNEE SYSTEM; PROSTHESIS, KNEE, PATELLOFEMOROTIBIA

Model Number	KC-36060
Health Effect - Clinical Code	Unspecified Infection (1930)
Date of Event	03/23/2021
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The complainant made no indication of any omnilife science device malfunction or deficiency related to the identity, quality, durability, reliability, safety, effectiveness or device performance contributing to the adverse event.Review of the manufacturing documentation and sterilization documentation for the devices in question revealed no deviation.
Event or Problem Description
A complaint was initiated for a patient who underwent a second knee revision surgery on (b)(6) 2021.The first revision surgery occurred on (b)(6) 2018 the original surgery date is (b)(6) 2017.The reason for revision is suspected infection.During the revision, the original femoral component, tibial baseplate, and patella were removed.During this revision, the tibial insert and retaining bolt from the first revision were also removed.All components were replaced with an antibiotic spacer, a femoral component and insert to hold the joint together.

• Brand Name: APEX KNEE SYSTEM
• Common Device Name: PROSTHESIS, KNEE, PATELLOFEMOROTIBIA
• Manufacturer (Section D): OMNILIFE SCIENCE, INC.; 480 paramount drive; raynham MA 02767
• MDR Report Key: 11683167
• Report Number: 1226188-2021-00048
• Device Sequence Number: 11496980
• Product Code: JWH
• UDI-Device Identifier: 00841690101802
• UDI-Public: 00841690101802
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K060192
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2018
• Device Explanted Year: 2021
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 04/17/2021

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: 08/31/2021
• Device Model Number: KC-36060
• Device Catalogue Number: KC-36060
• Device Lot Number: 24261
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 03/24/2021
• Initial Report FDA Received Date: 04/17/2021
• 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