FLEXCERA SMILE -a Dental resins for the fabrication of artificial teeth
FDA Recall Z-0643-2022 · Posted None
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Recalling FirmEnvisiontec US Llc
Recall StatusOpen, Classified
Product CodeEBI
Date Initiated2022-01-06
Product Quantity795 units
Reason for Recall
Manufactured in a non-FDA-registered manufacturing facility and product mislabeled as being of German origin
Firm Action
ENVISIONTEC US LLC issued Urgent Medical Device Recall letter on Jan 6, 2022. Letter states reason for recall, health risk and action to take:
1. Stop dispensing and distributing and quarantine these lots.
2. Please carry out a physical count and record this data on the Products Recall Response
Form included with this letter.
3. Submit the Products Recall Response Form via email or fax even if you do not have the
recalled product.
4. Contact Sedgwick as instructed in the Products Recall Response Form and return the
recalled product to:
Sedgwick
Attn: Event 7788
2670 Executive Dr., Suite A
Indianapolis, IN 46241
Notifications of this recall are being sent to all direct accounts of EnvisionTec US LLC For customers that redistribute this product to other accounts, please notify your accounts. No other lots, packages, or formulations are being recalled. For shipping assistance or questions about the recall process please contact Sedgwick at 1-888-759-6907 (phone), 1-866-462-9941 (fax) and [email protected]. For other inquiries regarding these products, please contact EnvisionTec customer service at nvisiontec.com/support.
Root Cause
Nonconforming Material/Component
Distribution Pattern
US Nationwide distribution.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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