PrepStain Syringing Pipettes 240 (Catalog #490517)
FDA Recall Z-1811-2012 · Posted 2012-06-15
Recalling FirmTripath Imaging, Inc.
Recall StatusTerminated
Product CodeMKQ
Date Initiated2012-03-22
Date Terminated2012-12-03
Product Quantity46,112,784 for all products in Recall Event
Reason for Recall
The PrepStain Syringing Pipettes may not dispense the minimum volume of 7.5 mL of the sample due to leaking. This event resulted in an increase in complaints of leaking syringing pipettes
Firm Action
BD Diagnostics sent a "BD PrepMate Syringing Pipette" letter dated March 2012 to all affected customers. The letter identified the product, problem, and actions to be taken by the customers. The firm encouraged customers to refer to the Operator's Manual and inspect the centrifuge tubes to verify that the correct amount of sample has been transferred. Customers experiencing this issue were instructed to discard the pipettes and contact BD Diagnostic Technical Support for a replacement. Contact the firm at 1-877-822-7771 for questions regarding this notice.
Root Cause
Component design/selection
Distribution Pattern
Worldwide Distribution.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.