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Bard Peripheral Vascular Inc recalls PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF 18295
Recalled May 19, 2021 · FDA recall Z-1550-2021 · Bard Peripheral Vascular
Hazard
Catheters may experience difficulty in flushing, infusion, and/or aspiration, and septum dislodgements. · FDA Class II
Units
2,194 units
Sold at
US Nationwide distribution in the states of AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN MO, NC, NE, NH, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV.
Description
Catheters may experience difficulty in flushing, infusion, and/or aspiration, and septum dislodgements.
Product
PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF 1829500, UDI: (01) 00801741027185 - Product Usage: The port system can be used for infusion of medications, I.V. fluids, parenteral nutrition solutions, blood products, and for the withdrawal of blood samples.
Manufacturer(s)
Bard Peripheral Vascular Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →