Z-2069-2017 Class II Terminated

Recalled by Almore International Inc — Beaverton, OR

Recall Details

Product Type
Devices
Report Date
May 17, 2017
Initiation Date
April 20, 2017
Termination Date
August 22, 2017
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1773 devices (US =1570; International = 203)

Product Description

Microfil Composite Instruments are packaged in an unsealed plastic sleeve, which is then placed in a cardboard box. Microfil Composite Instruments are intended to be sterilized by the dentist prior to each use. It is used for composite restoration development. The thin paddles shape light-cured composites. Paddles slide under the gum line to shape the margin. The flat ends contour the surfaces of the teeth and the thin edge is used to create esthetic highlights. Models: #96041  Gold Microfil #96042  Green Microfil #96043  Blue Microfil #96044  Set of 3 Microfil (Gold, Green, Blue)

Reason for Recall

Microfil Composite Instruments were distributed with a sterile symbol on their packaging label inserts, indicating that the products are sold as sterile devices. These products are not sterile and they are intended to be sterile prior to each use.

Distribution Pattern

Worldwide distributed - US Nationwide in AZ, CA, CO, CT, FL, GA, IA, IL, IN, MA, MN, MO, NC, NJ, NV, NY, OH, PA, TN, TX, WA, and WI, and internationally in Canada, Netherlands, and South Korea.

Code Information

no lot codes