RecallDepth

Article No. NA6050411, Valiant PhD No. 1 Econo

This recall is currently active, issued February 7, 2024. It was issued by Ivoclar Vivadent, Inc..

Company
Ivoclar Vivadent, Inc.
Recall Initiated
December 21, 2023
Posted
February 7, 2024
Recall Number
Z-1006-2024
Quantity
2 boxes (500 per box)
Firm Location
Amherst, NY
Official Source
View on FDA website ↗

Reason for Recall

Affected product may not perform as expected; the amalgam powder may not triturate correctly and the physical properties (i.e. strength, compression, working time, etc.) will be adversely affected.

Distribution

US Nationwide distribution in the states IN and TN.

Lot / Code Info

UDI-DI D707NA60504110, Lot Z066SD

Root Cause

Employee error

Action Taken

On December 19, 2023, the firm notified customers by phone. On December 21, 2023, the firm further notified affected customers via URGENT MEDICAL DEVICE RECALL letters through email. Customers were instructed to check their inventory for the affected lot and quarantine the product, and stop deliveries of the affected lot. Customers should respond to the letter and return all stock of affected product to the recalling firm. If product was further distributed, the customer should provide downstream customers' information to the recalling firm so that the firm may communicate recall information to them directly. Firm stated that product manufactured after December 6, 2023, were corrected for any irregularities. Customers with questions about risk minimizing safety measures may contact customercare.vigilance@ivoclar.com. For questions regarding replacement or credit note for products affected by this field safety notice, please contact customer service at Ivoclar Vivadent Inc at 1-800-533-6825.

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