Veridex, LLC CellSearch Circulating Tumor Cell Kit (Epithelial) IVD REF 7900001 Veridex LLC, a Johnson & Johnson Company. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
CellSearch Circulating Tumor Cell Kit (Epithelial) IVD REF 7900001 Veridex LLC, a Johnson & Johnson Company.
Brand
Veridex, LLC
Lot Codes / Batch Numbers
Lot number 0019, Exp 1/8/2010, 0019B, Exp 1/8/2010, 0039, Exp 3/16/2010, 0059, Exp 3/6/2010, 0079, Exp 2/20/2010, 0099, Exp 6/24/2010.
Products Sold
Lot number 0019, Exp 1/8/2010; 0019B, Exp 1/8/2010; 0039, Exp 3/16/2010; 0059, Exp 3/6/2010, 0079, Exp 2/20/2010; 0099, Exp 6/24/2010.
Veridex, LLC is recalling CellSearch Circulating Tumor Cell Kit (Epithelial) IVD REF 7900001 Veridex LLC, a Johnson & Johnson due to Veridex has received 4 complaints regarding reagent bottles having been incorrectly placed or duplicate bottles places within the reagent tray of Cell. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Veridex has received 4 complaints regarding reagent bottles having been incorrectly placed or duplicate bottles places within the reagent tray of CellSearch Circulating Tumor Cell Kit. Delayed detection of disease relapse or progression may occur due to false low CTC results.
Recommended Action
Per FDA guidance
Urgent Product Correction Notification letters were sent to all customers on August 12, 2009 by Federal Express. Customers were advised to inspect the kits to assure the proper reagents are in the proper position. If not, do not use the kits and contact the company at 877-837-4339 (chose option 1).
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
IN, MD
Page updated: Jan 10, 2026