ClearanceBrief
Recall Z-0618-2007 ยท FPA Set, Administration, Intravascular

Baxter Healthcare Corp.

Baxter Clearlink System Vented Paclitaxel Set; a sterile fluid pathway with polyethylene lined tubing, non-DEHP 12 inch pump segment, 0.22 micron downstream high pressure filter, Luer activated valve, male Luer lock adapter; for use with rigid nonvented solution containers on Colleague and Flo-Gard 6201 and 6301 series pumps; Baxter Healthcare, Deerfield, IL 60015; product code 2C8857

DateMar 14, 2007 (initiated Feb 16, 2007)
StatusTerminated
ReasonBaxter has received reports of disconnections/leaks during use of vented Paclitaxel administration sets.
Root causeOther
ActionBaxter sent the 2/16/07 Urgent Product Recall letter to affected customers, to the attention of the Director of Nursing with copies to the Materials Manager, via first class mail to advise them of the potential disconnections/leaks during use of the Vented Paclitaxel Administration Sets. The accounts were instructed to immediately discontinue use and segregate the listed affected lot numbers, and contact Baxter Center for Service at 1-888-229-0001 to arrange for the return and credit for the affected product. Any questions were directed to the Center for One Baxter at 1-800-422-9837.
Quantity480 units
DistributionWorldwide, including Switzerland, Australia, Canada, Hong Kong, India, Korea, Mexico, Malaysia, New Zealand, Panama, Phillipines, Singapore, Thailand and Taiwan.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K003225SOLUTION ADMINISTRATION SETS WITH CAPLESS LUER ACTIVATED VALVE
Baxter Healthcare Corp, Oct 19, 2000
K981792SOLUTION ADMINISTRATION SET
Baxter Healthcare Corp, Aug 17, 1998