Recall Z-1053-2012

Leica Microsystems, Inc. · initiated January 10, 2012

Terminated

Product

Leica Bond Ready-to-Use Primary Antibody CD7 (LP15) Reagent; 7 mL vial; an in vitro diagnostic monoclonal antibody for use as part of an antibody panel for the classification of tumors of T-cell origin; Catalog No. PA0266; Leica Biosystems Newcastle Ltd., Balliol Business Park West, Benton Lane, Newcastle Upon Tyne NE12 8EW, United Kingdom. For the qualitative identification by light microscopy of CD7 molecule in formalin-fixed, paraffin-embedded tissue by immunohistochemical staining using the automated Bond system.

Codes / lots: Catalog No. PA0266, lot numbers 10604 and 13566

Reason for recall

The primary antibodies to CD2 (clone 11F11) and CD7 (clone LP15) have been adulterated.

FDA-determined cause: Labeling mix-ups

Action taken

Leica Microsystems, Inc. sent a Medical Device Field Notification letter dated January 4, 2012, via first class mail on January 10, 2012, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer. Customers were instructed to discontinue use of the product and to return the product to the firm. Customers who have received the affected lot numbers of the listed products were requested to return any unused/part used reagents to the Buffalo Grove, IL, location for replacement. The accounts were asked to complete the attached Acknowledgement Form, acknowledging receipt and understanding of the letter, listing the lot numbers of the units at their facility and fax it back to Leica at 1-847-607-3147. Additional questions should be addressed to the account's Leica Representative. For further questions please call (847) 405-0123

Details

Recall number
Z-1053-2012
Initiated
January 10, 2012
Posted by FDA
February 17, 2012
Terminated
April 18, 2012
Product code
NJT – Immunohistochemistry Reagents And Kits
Quantity
139 - 7 mL vials
Distribution
Worldwide Distribution -- USA (nationwide) and the country of Canada.
Recalling firm
Leica Microsystems, Inc., Buffalo Grove, IL

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-1052-2012 Leica Bond Ready-to-Use Primary Antibody CD2 (11F11); 7 mL vial; an in vitro diagnostic…The primary antibodies to CD2 (clone 11F11) and CD7 (clone LP15) have been adulterated. 01/10/2012Terminated
Z-1054-2012 Novocastra Liquid Concentrated Mouse Monoclonal Antibody CD7 (LP15) Reagent; an in vitro…The primary antibodies to CD2 (clone 11F11) and CD7 (clone LP15) have been adulterated. 01/10/2012Terminated