Atlas FDA

Product names: a) Alginate Dental Impression Material Regular Set, Cinnamon Flavor, Pink Color b) Alginate Dental Impres

FDA device recall Z-0128-06 · posted 2005-11-05 · Terminated

Recall details

Recalling firm
Rite-Dent Manufacturing Corp.
Reason for recall
At least two of the ingredients used in the production of these products were not intended for human use. The ingredients are not listed in the master formula for these products nor are they listed on the ingredients list.
Action taken
The recall letter was sent to customers during the week of 9/26/05. The letters were sent via first class mail for domestic accounts and included a response card. A letter will also be translated into Spanish for Central American customers who will be asked to destroy inventory and return any products at their site and forward confirmation to Rite-Dent of the destruction. The recall letters request that distributors contact their customers and that retailers 'make every effort to contact their accounts'. The firm will contact non-responders. Returned product will be held at Rite-Dent for destruction after FDA notification.
Root cause
Process design
Status
Terminated
Product code
EHY
Quantity affected
74460 LBS
Distribution
Distributed throughout the Continental United States and to several countries in the Caribbean and Central America.
Date initiated
2005-09-21
Date posted
2005-11-05
Date terminated
2012-07-10
Location
Hialeah, FL

Monitor recalls programmatically

Recalls and clearances share one API, with change alerts when new recalls post.

Related 510(k) clearances

RecordFirmDate
ALGINATE IMPRESSION MATERIAL (K003426)Rite-Dent Manufacturing Corp.2001-01-23