Recall Z-0582-2026

Straumann USA LLC · initiated October 17, 2025

Class II Open, Classified

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

Emdogain; Article Numbers: (1) 440.230V10, (2) 475.132V10;

Codes / lots: 1. Article Number: 440.230V10; UDI-DI: N/A; Lot Numbers: EPZM8, HPT6, KEWN9, NAAM6, VAW80; 2. Article Number: 475.132V10; UDI-DI: N/A; Lot Numbers: CRL56, HPHJ1;

Reason for recall

The possibility for this product that is intended for demonstration purposes only to be placed in patients.

FDA-determined cause: Under Investigation by firm

Action taken

On October 17, 2025 Urgent Field Safety Action letters were sent to customers. Action to be taken: 1. 1. Check your inventory for the affected article/lot numbers. If the article is still in your inventory, then stop use/ distribution of the product immediately and quarantine / segregate physically. Please return the affected items to the attention of Jennifer Jackson at Straumann USA, LLC for credit as indicated on the Customer Confirmation Form. 2. 2. In all cases, complete and return the enclosed Customer Confirmation Form with the affected product using the return UPS label provided. Transmission of the Field Safety Notice This notice needs to be passed on to all those who need to be aware within your organization or to any organization where the affected devices have been transferred. The Food and Drug Administration (FDA) has been informed about this Field Safety Corrective Action. We apologize for any inconvenience that this may cause.

Details

Recall number
Z-0582-2026
Initiated
October 17, 2025
Posted by FDA
November 21, 2025
Product code
NQA – Biologic Material, Dental
Quantity
61 units
Distribution
US Nationwide distribution in the states of AZ, CA, DE, FL, ID, MO, TN, TX, UT, VA.
Recalling firm
Straumann USA LLC, Andover, MA

Official FDA recall record