Baxter Healthcare Corp.: Medical Device Recall in 2013 - (Recall #: Z-1601-2013)

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: Multirate Infusor Devices. Indicated for the intravenous administration of medications.

Product Classification:

Class II

Date Initiated: June 7, 2013

Date Posted: July 3, 2013

Recall Number: Z-1601-2013

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: 2C1154KP, 2C1155KP, 2C9960KP, 2C9961KP Lot Numbers: 10F030 10F066 10H043 10H104 10K027 10K099 10M090 10G028 10J059 10M019 10M089 10F058 10G069 10G042 10J048 10M026 Expiration Date: 06/30/13

Distribution Pattern:

Distributed Nationwide and in Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated