FDA Recall Terminated

i-STAT ACT Celite Cartridges in vitro diagnostic test used to monitor moderate and high-level heparin therapy through analysis of arterial and venous whole blood samples.

Recall: Z-0399-2011 · Initiated October 6, 2010

Recall

Recall Number
Z-0399-2011
Event Number
57005
Firm
Abbott Point Of Care Inc.
FEI Number
2245578
Product Code
JBP
Status
Terminated
Root Cause
Other
Initiated
October 6, 2010
Posted
November 17, 2010
Terminated
August 22, 2012
Address
400 College Rd E, Princeton, NJ, 08540-6607

Description

i-STAT ACT Celite Cartridges in vitro diagnostic test used to monitor moderate and high-level heparin therapy through analysis of arterial and venous whole blood samples.

Reason

Certain lots of i-STAT Celite ACT and Kaolin ACT cartridges may be difficult to fill or will not fill when attempting to transfer blood to the sample entry port of the cartridge.

Action

Abbott Point of Care, Inc. sent an URGENT RECALL NOTICE dated September 2010 on October 6, 2010 by Federal Express to all US customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to discontinue use of cartridges from the identified lots. If customers did not currently have replacement cartridges then they should continue to use the cartridge lot until their facility receives replacement material. Upon receipt of replacement material, customers were to discontinue use of and return the affected cartridges and switch to the replacement material. All unused cartridges will be credited and will be returned. If you have any questions regarding this information, please contact Abbott Point of Care Technical Support at 800-366-8020, Option 1 or your Abbott Point of Care representative.

Distribution

Worldwide Distribution

Quantity

49,025 cartridges.