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Access Scientific LLC recalls BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 4Fr 10cm Max Barrier Kit. REF/UDI / 94107/10859821006206
Recalled May 20, 2020 · FDA recall Z-1977-2020 · Access Scientific
Hazard
Saline Flush Syringe compromised sterility due to holes in the packaging. · FDA Class II
Units
2,055 units
Sold at
US Nationwide distribution including in the states of AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, ME, MI, MN, MO, MS, NC, NH, NJ, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, WA.
Description
Saline Flush Syringe compromised sterility due to holes in the packaging.
Product
BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 4Fr 10cm Max Barrier Kit. REF/UDI / 94107/10859821006206 - Product Usage: is used to gain access to the vascular system to sample blood and administer fluids intravenously. It may be used for power injection of contrast media up to a rate of 8 ml/sec and at a maximum of 325 psi fluid pressure.
Manufacturer(s)
Access Scientific LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →