MAUDE Adverse Event Report: ZIMMER ORTHOPAEDIC MFG. LTD. FEMUR CEMENTED POSTERIOR; PROSTHESIS, KNEE

Model Number	N/A
Medical Device Problem Code	Unstable (1667)
Health Effect - Clinical Codes	Inflammation (1932); Pain (1994); Swelling (2091)
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
(b)(4).Customer has indicated that the product will not be returned to zimmer biomet for investigation, as the device remains implanted.The investigation is in process.Once the investigation has been completed, a follow-up mdr will be submitted.Implant date: (b)(6) 2018.Concomitant medical products: 42512400716, articular surface, lot # 63052412; 42532007101, tibia, lot # 63548612; 42540000032, poly patella, lot # 63634814.Multiple mdr reports were filed for this event, please see associated reports: 0001822565-2019-04633, 0001822565-2019-04635, 0002648920-2019-00785,.
Event or Problem Description
It was reported that approximately 17 months post implantation, the patient was experiencing pain, swelling, inflammation, and instability in the left knee.Attempts have been made and no further information has been provided.
Event or Problem Description
It was reported that approximately 2.5 years post implantation, the patient is experiencing pain, swelling, inflammation, and instability.The patient has now been indicated for a revision due to aseptic loosening.
Additional Manufacturer Narrative
This follow-up report is being submitted to relay additional information.If any further information is found which would change or alter any conclusions or information, a supplemental will be filed accordingly.Zimmer biomet will continue to monitor for trends.
Additional Manufacturer Narrative
This follow-up report is being submitted to relay additional information.The product was evaluated through manufacturing review and the reported event was confirmed through review of medical records.The device history records were reviewed and no discrepancies were identified.Per package insert for persona, pain, swelling, loosening, instability, poor range of motion are known adverse effects of these systems.However, a definitive root cause could not be determined with the information provided.If any further information is found which would change or alter any conclusions or information, a supplemental will be filed accordingly.Zimmer biomet will continue to monitor for trends.
Event or Problem Description
No further event information available at the time of this report.

• Brand Name: FEMUR CEMENTED POSTERIOR
• Common Device Name: PROSTHESIS, KNEE
• Manufacturer (Section D): ZIMMER ORTHOPAEDIC MFG. LTD.; building no 2 east park; shannon industrial estate; shannon, county clare ; EI
• MDR Report Key: 9252277
• Report Number: 3007963827-2019-00307
• Device Sequence Number: 19333512
• Product Code: JWH
• UDI-Device Identifier: 00889024228771
• UDI-Public: (01)00889024228771
• Combination Product (Y/N): N
• Initial Reporter State: MO
• Initial Reporter Country: US
• PMA/510(K) Number: K113369
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• Reporter Type: Manufacturer
• Report Source: consumer
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 04/01/2020

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
• Operator of Device: Health Professional
• Device Expiration Date: 12/31/2025
• Device Model Number: N/A
• Device Catalogue Number: 42500006401
• Device Lot Number: 63239722
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: No
• Initial Date Received by Manufacturer: 10/14/2019
• Supplement Date Received by Manufacturer: 11/03/2019; 03/31/2020
• Initial Report FDA Received Date: 10/29/2019
• Supplement Report FDA Received Date: 11/18/2019; 04/01/2020
• 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: Other
• Patient Weight: 136