MAUDE Adverse Event Report: BIOMET UK LTD. OXF UNI TIB TRAY SZ B LM PMA; KNEE PROSTHESIS

Catalog Number 154720

Device Problems Collapse (1099); Appropriate Term/Code Not Available (3191)

Patient Problem No Information (3190)

Event Date 09/24/2018

Event Type  Injury  

Manufacturer Narrative

(b)(4).Medical product - oxf twin-peg cmntd fem xs pma, item 161467, lot 3021395.Therapy date - (b)(6) 2018.Medical product - oxf anat brg lt x-sm sz 5 pma, item 159792, lot 85320.Therapy date - (b)(6) 2018.The investigation is in process.Once the investigation has been completed, a follow-up mdr will be submitted.

Event Description

It was reported that a patient underwent an initial knee procedure and subsequently the patient was revised due to lateral compartment collapse.

Manufacturer Narrative

(b)(4).Reported event was unable to be confirmed due to limited information received from the customer.Device history record (dhr) was reviewed and no discrepancies were found.Root cause was unable to be determined as the necessary information to adequately investigate the reported event was not 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 Description

It was reported that a patient underwent an initial knee procedure and subsequently the patient was revised due to lateral compartment collapse.

• Brand Name: OXF UNI TIB TRAY SZ B LM PMA
• Type of Device: KNEE PROSTHESIS
• Manufacturer (Section D): BIOMET UK LTD.; waterton industrial estates; bridgend CF31 3XA; UK CF31 3XA
• MDR Report Key: 8001127
• MDR Text Key: 124886977
• Report Number: 3002806535-2018-01155
• Device Sequence Number: 0
• Product Code: NRA
• PMA/PMN Number: P010014
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: health professional
• Type of Report: Initial,Followup
• Report Date: 01/29/2019

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 10/24/2018
• Is this an Adverse Event Report?: Yes
• Device Operator: Health Professional
• Device Expiration Date: 03/31/2024
• Device Catalogue Number: 154720
• Device Lot Number: 317790
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: No
• Date Manufacturer Received: 01/01/2019
• Is This a Reprocessed and Reused Single-Use Device?: No
• Removal/Correction Number: N/A
• Patient Sequence Number: 0
• Patient Outcome(s): Hospitalization; Required Intervention