FDA Recall Terminated

Breeze Self-Adhesive Resin Cement, part number: N97F. The intended use is for cementation of porcelain, resin, and metal-based inlays, onlays, crowns, bridges, and posts.

Recall: Z-1100-2012 · Initiated December 2, 2010

Recall

Recall Number
Z-1100-2012
Event Number
61235
Firm
Kerr Corporation
FEI Number
2024312
Product Code
EMA
Status
Terminated
Root Cause
Nonconforming Material/Component
Initiated
December 2, 2010
Posted
February 24, 2012
Terminated
February 24, 2012
Address
1717 W Collins Ave, Orange, CA, 92867-5422

Description

Breeze Self-Adhesive Resin Cement, part number: N97F. The intended use is for cementation of porcelain, resin, and metal-based inlays, onlays, crowns, bridges, and posts.

Reason

The recall was initiated because Pentron Clinical has confirmed that the Breeze Self-Adhesive Resin Cement exhibits faster than expected gel and set times. If the work time is exceeded when using this material, it could possibly result in inadequate bond strength.

Action

An "Urgent Medical Device Recall" letter was sent on 12/17/2010 via USPS 1st class mail to all their customers. The letter provides the customers with an explanation of the problem identified and the action to be taken. Customers were instructed to complete and fax back the enclosed recall return form. Customers with questions were instructed to call (800) 551-0283.

Distribution

Worldwide Distribution - Nationwide (USA) and the countries of Vietnam, Jordan,Turkey, and Italy.

Quantity

622 units total (12 units in US)