MAUDE Adverse Event Report: ZIMMER MANUFACTURING B.V. ALL POLY PATELLA; PROSTHESIS KNEE

Model Number N/A

Device Problem Naturally Worn (2988)

Patient Problems Failure of Implant (1924); Loss of Range of Motion (2032)

Event Date 01/11/2024

Event Type  Injury  

Manufacturer Narrative

(b)(4).D10 - medical product: articular surface medial congruent (mc) catalog # 42522100716 lot # 63846189.G2: australia.Multiple mdr reports were filled for this event: 3007963827-2024-00025.H3: customer has indicated that the product will not be returned because product location is unknown.The investigation is in process.Once the investigation has been completed, a follow-up mdr will be submitted.H3 other text : product location unknown.

Event Description

It was reported patient underwent a revision procedure two years post implantation due to range of motion and implant wear.No more information is available.

• Brand Name: ALL POLY PATELLA
• Type of Device: PROSTHESIS KNEE
• Manufacturer (Section D): ZIMMER MANUFACTURING B.V.; turpeaux industrial park; route #1 km 123.4 bldg #1; mercedita PR 00715
• Manufacturer (Section G): ZIMMER MANUFACTURING B.V.; turpeaux industrial park; route #1 km 123.4 bldg #1; mercedita PR 00715
• Manufacturer Contact: jennifer rapsavage ; 56 e. bell dr.; warsaw, IN 46582 ; 5745260384
• MDR Report Key: 18613095
• MDR Text Key: 334201576
• Report Number: 0002648920-2024-00026
• Device Sequence Number: 1
• Product Code: MBH
• UDI-Device Identifier: 00889024247697
• UDI-Public: (01)00889024247697(17)260418(10)64941142
• Combination Product (y/n): N
• Reporter Country Code: AS
• PMA/PMN Number: K121771
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Foreign,Health Professional,Company Representative
• Reporter Occupation: Physician
• Type of Report: Initial
• Report Date: 01/31/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 01/31/2024
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: N/A
• Device Catalogue Number: 42540200032
• Device Lot Number: 64941142
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Date Manufacturer Received: 01/11/2024
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 06/16/2021
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Removal/Correction Number: N/A
• Patient Sequence Number: 1
• Treatment: SEE H10 NARRATIVE
• Patient Outcome(s): Required Intervention; Hospitalization
• Patient Sex: Female
• Patient Weight: 102 KG