Baxter Healthcare Corp.: Medical Device Recall in 2013 - (Recall #: Z-1606-2013)

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: Basal/Bolus Infusor. Indicated for the intravenous administration of medications.

Product Classification:

Class II

Date Initiated: June 7, 2013

Date Posted: July 3, 2013

Recall Number: Z-1606-2013

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: 2C1955KJP, 2C1976KJ Lot Codes: 08K006 08M038 08N001 09C021 09E028 09F078 09H080 09J046 09M052 09N030 09N048 10A043 108023 10E054 10H055 10J031 10K050 10M085 10N026 09H033 10B028 10B081 10E004 10J106 Expiration Dates: 06/30/15, 12/31/14, 12/31/15, 06/30/14, 12/31/14

Distribution Pattern:

Distributed Nationwide and in Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated