Baxter Healthcare Corp.: Medical Device Recall in 2013 - (Recall #: Z-1603-2013)

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:

Brand Name: Intermate Infusion Pump. Indicated for the intravenous administration of medications.

Product Classification:

Class II

Date Initiated: June 7, 2013

Date Posted: July 3, 2013

Recall Number: Z-1603-2013

Event ID: 65365

Reason for Recall:

Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall for the products listed above due to an increase in rupture complaints. Baxter has implemented product and process improvements which have substantially improved product quality. Complaint rates for ruptures have since decreased. Baxter wants to ensure that no affected product remains in the field.

Status: Terminated

Product Quantity: 3,255,096 total

Code Information:

Product Codes: 2C1064K Lot Codes: 10F007 10F077 10H075 10J097 10K076 10K112 10M062 Expiration Date: 06/30/13

Distribution Pattern:

Distributed Nationwide and in Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated