FDA Recall Terminated

Luminesse ML PMMA, 98x20mm, REF: 5336-B1 - Product Usage: used as a milling blank in the fabrication of provisional crowns and bridges. All blanks are solely used by a Trained Dental Technician or on the order of a dental professional.

Recall: Z-0512-2021 · Initiated October 9, 2020

Recall

Recall Number
Z-0512-2021
Event Number
86614
Firm
Talladium Inc
FEI Number
2023129
Product Code
EBG
Status
Terminated
Root Cause
Labeling mix-ups
Initiated
October 9, 2020
Terminated
August 17, 2022
Address
27360 Muirfield Ln, Valencia, CA, 91355-1010

Description

Luminesse ML PMMA, 98x20mm, REF: 5336-B1 - Product Usage: used as a milling blank in the fabrication of provisional crowns and bridges. All blanks are solely used by a Trained Dental Technician or on the order of a dental professional.

Reason

Heat-cured polymethylmethacrylate (PMMA) milling blank product used to make long-term temporary crowns and bridge restorations has incorrect label. label states Part no. 5336-B1 (98x20mm). However, the item inside the box was Part no. 4302-B1 (95x20mm). An incorrect label may result in compatibility issues when setting up the disc with milling machine fixtures due to size variation.

Action

On 10/09/20, Urgent Medical Device Recall notices were mailed and/or emailed to customers. Customers were asked to do the following: 1) Check your stock and quarantine the affected stock on hand to prevent further use. 2) Using the provided customer letter and Recall Acknowledgement Form templates, communicate this recall to any of your customers who have received product included within the scope of the recall. 3) Return product, complete the enclosed Recall Acknowledgement Form, scan and email to [email protected] Complete the attached Acknowledgement form even if you do not have any affected stock, scan and email. The following contact information was provided: 800-221-6449 and www.TALLADIUM.com

Distribution

U.S. Nationwide distribution including in the states of PA, KS, OR, FL, CA.

Quantity

10