The Binding Site Group, Ltd.: Medical Device Recall in 2017 - (Recall #: Z-1055-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Digital RID Plate Reader and Software Product Code: AD400

Product Classification:

Class II

Date Initiated: October 9, 2012

Date Posted: January 25, 2017

Recall Number: Z-1055-2017

Event ID: 76043

Reason for Recall:

If a control ring is marked after reading, the software will not flag results that are out of the specified QC range.

Status: Terminated

Product Quantity:

Code Information:

UDI 05051700000376

Distribution Pattern:

U.S. distribution to the following; MA, GA, NY, IA, CA, IL, UT, NJ, NC, MD, MN. Foreign distribution to the following; UK, Germany, Spain, France.

Voluntary or Mandated:

Voluntary: Firm initiated