FDA recall record

Baxter Healthcare Mini-Infuser Model 300XL Multispeed Infusion Pump, an Rx battery operated recall — FDA Z-2269-2012

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…

Class IIIclassification
Z-2269-2012official record ID
Sep 5, 2012report date

Recall record at a glance

Official recordZ-2269-2012
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmBaxter Healthcare Corp.
Report dateSep 5, 2012
Recall initiation dateMar 4, 2011
Quantity19,380 units
LocationRound Lake, IL, United States

Official product description

Mini-Infuser Model 300XL Multispeed Infusion Pump, an Rx battery operated syringe infusion pump with an active time scale and rate selector switch; product codes 2M8171 and 2M8171R. 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.

Why the product was recalled

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

Distribution information

45,865 units

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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About this record

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