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C.R. Bard, Inc. recalls HydroSil Gripper Intermittent Catheters- 10" lengths - 30 catheters per box, each catheter is packaged in an individual
Recalled April 11, 2018 · FDA recall Z-1307-2018 · C.R. Bard
Hazard
Several instances of a catheter caught in the sterile barrier seal and in some instances cut catheters were observed. · FDA Class II
Units
44640.0 units
Sold at
US Nationwide in the states of AK, AL, AR, AZ, CA, FL, GA, HI, IA, ID, KS, KY, MD, ME, MI, MN, MO, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV, including Puerto Rico
Description
Several instances of a catheter caught in the sterile barrier seal and in some instances cut catheters were observed.
Product
HydroSil Gripper Intermittent Catheters- 10" lengths - 30 catheters per box, each catheter is packaged in an individual pouch. MGC3 Product Usage Intermittent catheters are intended for urinary bladder drainage in patients requiring catheterization for management of incontinence, voiding dysfunction, and surgical procedures.
Manufacturer(s)
C.R. Bard, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →