FDA Recall Open, Classified

Article No. NA6050411, Valiant PhD No. 1 Econo

Recall: Z-1006-2024 · Initiated December 21, 2023

Recall

Recall Number
Z-1006-2024
Event Number
93796
Firm
Ivoclar Vivadent, Inc.
FEI Number
1316092
Product Code
EJJ
Status
Open, Classified
Root Cause
Employee error
Initiated
December 21, 2023
Posted
February 7, 2024
Address
175 Pineview Dr, Amherst, NY, 14228-2231

Description

Article No. NA6050411, Valiant PhD No. 1 Econo

Reason

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.

Action

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 [email protected]. 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.

Distribution

US Nationwide distribution in the states IN and TN.

Quantity

2 boxes (500 per box)