ClearanceBrief
Recall Z-1308-2018 ยท EZD Catheter, Straight

C.R. Bard, Inc.

Magic 3 Intermittent Catheters- 12 Male - 30 catheters per box, each catheter is packaged in an individual pouch. Urinary catheter.

DateApr 4, 2018 (initiated Sep 14, 2017)
StatusTerminated
ReasonSeveral instances of a catheter caught in the sterile barrier seal and in some instances cut catheters were observed.
Root causeProcess control
ActionA notification letter was sent to four hundred and fourteen (414) consignees via Federal Express on September 15, 2017. The letter explained the problem and requested return of the product. Distributors were directed to cease distribution of the recalled products and notify their customers of the recall.
Quantity10,949,013 units in total
DistributionUS 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
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K000723HYDROPHILIC SILICONE FOLEY CATHETER AND PERSONAL CATHETER (HYDROPHILIC AND NON-HYDROPHILIC)
Rochester Medical Corp., May 19, 2000
K122785HYDROSIL; MAGIC; PERSONAL CATHETER
Rochester Medical Corp., May 14, 2013