Baxter Healthcare Corp. Rt. Baxter Interlink System Vented Paclitaxel Set; a sterile fluid pathway with polyethylene lined tubing, non-DEHP pump segment, 0.22 micron downstream high pressure filter, injection site, 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 2C7557 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Baxter Interlink System Vented Paclitaxel Set; a sterile fluid pathway with polyethylene lined tubing, non-DEHP pump segment, 0.22 micron downstream high pressure filter, injection site, 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 2C7557
Brand
Baxter Healthcare Corp. Rt.
Lot Codes / Batch Numbers
product code 2C7557, lots R06I12067, R06J07025, R06J19079, R06J20044
Products Sold
product code 2C7557, lots R06I12067, R06J07025, R06J19079, R06J20044;
Baxter Healthcare Corp. Rt. is recalling Baxter Interlink System Vented Paclitaxel Set; a sterile fluid pathway with polyethylene lined tubin due to Baxter has received reports of disconnections/leaks during use of vented Paclitaxel administration sets.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Baxter has received reports of disconnections/leaks during use of vented Paclitaxel administration sets.
Recommended Action
Per FDA guidance
Baxter 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.
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 noticePage updated: Jan 10, 2026