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Smiths Medical ASD Inc. recalls Medfusion Syringe Infusion Pump, containing the Barrel Clamp Guide mechanism
Recalled August 15, 2018 · FDA recall Z-2662-2018 · Smiths Medical ASD
Hazard
Certain Barrel Clamp Guides may contain a ridge that could potentially lead to spring slippage, resulting in the inability of the pump to recognize a loaded syringe or the pump, misidentifying the size of a loaded syringe. · FDA Class II
Units
276 units
Sold at
US distribution to AL, AZ, CA, DC, FL, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, NJ, NM, NY, OH, OK, PA, TN, TX, UT, VA, WA. International distribution to Canada and Lebanon.
Description
Certain Barrel Clamp Guides may contain a ridge that could potentially lead to spring slippage, resulting in the inability of the pump to recognize a loaded syringe or the pump, misidentifying the size of a loaded syringe.
Product
Medfusion Syringe Infusion Pump, containing the Barrel Clamp Guide mechanism
Manufacturer(s)
Smiths Medical ASD Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →