Emdogain; Article Numbers: (1) 440.230V10, (2) 475.132V10;
FDA Recall Z-0582-2026 · Posted 2025-11-21
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Recalling FirmStraumann USA LLC
Recall StatusOpen, Classified
Product CodeNQA
Date Initiated2025-10-17
Product Quantity61 units
Reason for Recall
The possibility for this product that is intended for demonstration purposes only to be placed in patients.
Firm Action
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.
Root Cause
Under Investigation by firm
Distribution Pattern
US Nationwide distribution in the states of AZ, CA, DE, FL, ID, MO, TN, TX, UT, VA.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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