MAUDE Adverse Event Report: ZIMMER ORTHOPAEDIC MFG. LTD. ARTICULAR SURFACE FIXED BEARING CRUCIATE RETAINING LEFT 12 MM; PROSTHESIS, KNEE

Model Number	N/A
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Pain (1994)
Date of Event	06/18/2021
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
(b)(4).Report source: new zealand.Customer has indicated that the product will not be returned to zimmer biomet for investigation, as the device was not returned by the patient.The investigation is in process.Once the investigation has been completed, a follow-up mdr will be submitted.Additional associated products and mdrs: 42502606201 femur cemented cruciate retaining standard left size 7 lot# 63840844 mdr: 3007963827-2021-00149.42532007101 natural tibia cemented 5 degree stemmed left size e lot# 64315382 mdr: 3007963827-2021-00150.
Event or Problem Description
It was reported a patient underwent an initial left knee arthroplasty.Subsequently, was revised one year, seven months post procedure due to pain.
Event or Problem Description
No further event information available at the time of this report.
Additional Manufacturer Narrative
This follow-up report is being submitted to relay additional information.No product was returned for evaluation.Visual examination of the provided pictures identified foreign material/debris on all the implants.Review of the device history record identified no deviations or anomalies during manufacturing.Radiographs were provided and reviewed by a health care professional.Review of the available records identified the following: lateral view demonstrates a thin periprosthetic lucency along the undersurface of the posterior tibial plate; hardware and bones appear intact with normal alignment; small to moderate sized suprapatellar joint effusion; overall fit, alignment, and bone quality appears normal.No confirmed findings related directly to the hardware that would contribute to pain.Complaint is not confirmed.A definitive root cause cannot be determined.No corrective actions, preventive actions, or field actions resulted after investigation of this event.

• Brand Name: ARTICULAR SURFACE FIXED BEARING CRUCIATE RETAINING LEFT 12 MM
• 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: 12154626
• Report Number: 3007963827-2021-00151
• Device Sequence Number: 4616265
• Product Code: JWH
• UDI-Device Identifier: 00889024235137
• UDI-Public: (01)00889024235137(17)220930(10)63772111
• Combination Product (Y/N): N
• Initial Reporter Country: NZ
• PMA/510(K) Number: K121771
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2019
• Device Explanted Year: 2021
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 07/21/2021

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?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 09/30/2022
• Device Model Number: N/A
• Device Catalogue Number: 42512000512
• Device Lot Number: 63772111
• Was the Report Sent to FDA?: No
• Initial Date Received by Manufacturer: 06/18/2021
• Supplement Date Received by Manufacturer: 07/19/2021
• Initial Report FDA Received Date: 07/12/2021
• Supplement Report FDA Received Date: 07/21/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• If action reported to FDA under 21 USC 360i(g), list FDA-assigned Recall Number or include a statement: N/A
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: SEE H10 NARRATIVE
• Outcome Attributed to Adverse Event: Hospitalization; Required Intervention
• Patient Weight: 95