Baxter Healthcare Corp.: Medical Device Recall in 2013 - (Recall #: Z-0109-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Vented Spike Adapter Product Code 2C0471, Sterile, nopyrogenic. Manufactured by an affiliate of Baxter Healthcare Corporation, Clintec Nutrition Division, Deerfield IL 60015 USA. An IV transfer device, used to transfer fluids in pharmacy compounding system.

Product Classification:

Class II

Date Initiated: August 30, 2013

Date Posted: November 6, 2013

Recall Number: Z-0109-2014

Event ID: 66222

Reason for Recall:

Potential tears in the pouch of six lots of Vented Spike Adapter Product Code 2C0471

Status: Terminated

Product Quantity: 49,344 units

Code Information:

R13D09024, R13D09107, R13D12101, R13D17068, R13D18066, R13D20070

Distribution Pattern:

Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated