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Recall Observatory FDA recall evidence

Device product

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.

Z-2268-2012

March 04, 2011

Class III

Product summary

Firm
Baxter Healthcare Corp.
Event
Event 62881
Status
Terminated
Classification
Class III
Quantity
26,485 units
Official record key
device-enforcement:Z-2268-2012

Official wording

Reason: 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

Code information: product codes 2M8170 and 2M8170R, all serial numbers

Distribution pattern: 45,865 units

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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