Baxter Healthcare Corp.: Medical Device Recall in 2016 - (Recall #: Z-2687-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Baxter Non-DEHP Micro-Volume Extension Set, Male Luer Lock Adapter, 36 (91 cm), Volume 0.32 mL; an Rx sterile, single use nonpyrogenic fluid pathway; 50 sets per case; For the administration of drugs and solutions to a patient's vascular system through a vascular access device.

Product Classification:

Class II

Date Initiated: December 14, 2012

Date Posted: September 7, 2016

Recall Number: Z-2687-2016

Event ID: 63898

Reason for Recall:

Some of the individual extension set packages were improperly sealed, compromising the sterility of the product.

Status: Terminated

Product Quantity: 15,257 units

Code Information:

product code 2N3345, lot number UR12E03108

Distribution Pattern:

Worldwide Distribution - US including FL, GA, IL, KS, KY, MI, MO, NC, ND, OH, PA, SC, TN, TX, WV, Puerto Rico and Internationally to Canada.

Voluntary or Mandated:

Voluntary: Firm initiated