Baxter Healthcare Corp.: Medical Device Recall in 2012 - (Recall #: Z-2268-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

Mini-Infuser Model 150XL Single Speed Infusion Pump, an Rx battery operated syringe infusion pump; Product Usage: These product codes includes refurbished units. Intended for the controlled rate delivery of small volume parental fluids as prescribed by a physician. Usage: The Mini-Infuser System is designed for controlled intermittent administration of intravenous medication.

Product Classification:

Class III

Date Initiated: March 4, 2011

Date Posted: September 5, 2012

Recall Number: Z-2268-2012

Event ID: 62881

Reason for Recall:

Should a battery with the minimum contact diameter (.51 inches) be placed on the battery spring (.53 inches), an electrical circuit will not be completed and the Mini-Infuser will not operate. The reason being that the Mini-Infuser Battery Spring has a flat contact that measures .53 inches ¿.01 inches on the inner diameter of the spring coil. The IEC 60086-2 and ANSI 08 standards specify a minimum

Status: Terminated

Product Quantity: 26,485 units

Code Information:

product codes 2M8170 and 2M8170R, all serial numbers

Distribution Pattern:

45,865 units

Voluntary or Mandated:

Voluntary: Firm initiated