FDA Recall Terminated

Is-anti-Gliadin IgG Enzyme Immunoassay Test Kit packaged in cardboard boxes with individual components secured within a foam insert. Catalog Number # 720-800. - Laboratory In-Vitro Diagnostic Assay intended for the semi-quantitative detection of IgG antibodies to Gliadin in human serum by indirect enzyme immunoassay as an aid in the diagnosis of celiac disease.

Recall: Z-1684-2008 · Initiated March 21, 2008

Recall

Recall Number
Z-1684-2008
Event Number
47430
Firm
Diamedix Corporation
FEI Number
1044713
Product Code
MST
Status
Terminated
Root Cause
Environmental control
Initiated
March 21, 2008
Posted
September 16, 2008
Terminated
February 11, 2009
Address
2140 N. Miami Avenue, Miami, FL, 33127

Description

Is-anti-Gliadin IgG Enzyme Immunoassay Test Kit packaged in cardboard boxes with individual components secured within a foam insert. Catalog Number # 720-800. - Laboratory In-Vitro Diagnostic Assay intended for the semi-quantitative detection of IgG antibodies to Gliadin in human serum by indirect enzyme immunoassay as an aid in the diagnosis of celiac disease.

Reason

Standards and controls in the Is-anti-Gliadin IgG Test Kits are exhibiting low activity. A drop in the O.D.s the Positive Control could potentially recover low out of range (which would invalidate the test), or false positive test results could be obtained.

Action

A Customer Notification Letter was sent to each customer via Certified Mail for domestic customers and via Federal Express for international customer requesting them to contact Diamedix Technical Services to arrange for the return and replacement of any kits of the lot in question. If you have any questions please contact Glenn Gerstenfeld at 1-800-327-4565 or (305) 324-2300.

Distribution

Class II Recall - Worldwide Distribution.

Quantity

174 Test Kits