Baxa Corporation: Medical Device Recall in 2013 - (Recall #: Z-1752-2013)

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:

ExactaMix 1200 and 2400 Compounders. Used as an automated pumping system that compounds multiple sterile ingredients into a finished solution.

Product Classification:

Class II

Date Initiated: June 4, 2013

Date Posted: July 24, 2013

Recall Number: Z-1752-2013

Event ID: 65215

Reason for Recall:

Baxter Healthcare is recalling certain ExactaMix automated compounding devices due to the complementary metal oxide semi-conductor battery failure resulting in resetting the internal clock of the device to midnight December 31, 2010.

Status: Terminated

Product Quantity: 753 units

Code Information:

ExactaMix 1200 serial numbers 45004-45481 (sequentially), and ExactaMix 2400 serial numbers 40005-40335.

Distribution Pattern:

Worldwide Distribution-USA (nationwide) including Puerto Rico, and the countries of Canada, Latin America, Europe/Middle East/Africa, and Taiwan.

Voluntary or Mandated:

Voluntary: Firm initiated