MAUDE Adverse Event Report: OMNILIFE SCIENE APEX KNEE SYSTEM; PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL

Catalog Number	KP-0035L
Medical Device Problem Code	Loosening of Implant Not Related to Bone-Ingrowth (4002)
Health Effect - Clinical Code	Aseptic loosening (4883)
Date of Event	08/24/2025
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The complainant made no indication of any omnilife science device malfunction or deficiency related to 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 from process or non-conformity of product that would have caused or contributed to the adverse event.This report is filed with the fda due to an adverse event experienced with a device that is similar to those placed on the market in the usa, however, this event occurred outside of the usa.The submission of this report does not constitute an admission that the device, reporting entity, entity's representative or distributor caused or contributed to this event.
Event or Problem Description
A complaint was initiated for a patient who underwent a knee revision surgery on (b)(6) 2025.The original surgery is dated (b)(6) 2014.The reason for revision is reported loosening.During the revision all implants were removed and replaced with non-omni implants.

• Brand Name: APEX KNEE SYSTEM
• Common Device Name: PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL
• Manufacturer (Section D): OMNILIFE SCIENE; 480 paramount drive; raynham MA 02767
• Manufacturer (Section G): OMNILIFE SCIENCE; 480 paramount dr; raynham MA 02767
• Manufacturer Contact: jamie demedeiros ; 480 paramount dr; raynham, MA 02767
• MDR Report Key: 22911018
• Report Number: 1226188-2025-00040
• Device Sequence Number: 9110941
• Product Code: JWH
• UDI-Device Identifier: 00841690112082
• UDI-Public: 00841690112082
• Combination Product (Y/N): N
• Initial Reporter Country: AS
• PMA/510(K) Number: K102578
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2014
• Device Explanted Year: 2025
• 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): 08/28/2025

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: 02/28/2014
• Device Catalogue Number: KP-0035L
• Device Lot Number: 16583
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/25/2025
• Initial Report FDA Received Date: 08/28/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 02/28/2014
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: REF: KC-2204L.LOT NUMBER: 15608.; REF: KC-40358.LOT NUMBER: 18683.; REF: KP-20010.LOT NUMBER: 18696.; REF: KP-20310.LOT NUMBER: 18443.
• Outcome Attributed to Adverse Event: Required Intervention; Hospitalization
• Patient Sex: Female