ClearanceBrief
Recall Z-3116-2026 ยท MJC Catheter, Urological (Antimicrobial) And Accessories

C.R. Bard Inc

Products that contain the Pericare Wipes: *Bardex I.C. Complete Care Foley Catheter Tray REF: 300316A UDI codes: 00801741024344 10801741024341 *Bardex I.C. Complete Care Foley Catheter Tray and Urine Meter REF: 303314A 303316A 303318A UDI code: 00801741024252 10801741024259 00801741024269 10801741024266 00801741024276 10801741024273 *SureStep" Foley Tray System Bardex IC Complete Care REF: A300

DateSep 4, 2026 (initiated Jun 25, 2026)
StatusOpen, Classified
ReasonDue to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.
Root causeUnder Investigation by firm
ActionOn 06/25/2026, an "URGENT Medical Device Recall" Letter was via regional courier services or other electronic means to inform customers that based on customer feedback, BD has identified that the CliniClean Pericare Wipes provided within Urinary Catheter Trays may be potentially contaminated with an unknown non-biological substance. Customer are instructed to: Do not use CliniClean Pericare Wipes contained within the affected products listed in Attachment 2. The CliniClean Pericare Wipes are the only impacted component within the tray and all remaining components can continue to be safely use
Quantity212580
DistributionWorldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI and WY. The countries of Bahrain, Canada, Cos
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K040658BARDEX I.C. LATEX FOLEY CATHETER
C.R. Bard, Inc., Sep 29, 2004
K910318BARD(R) HYDROGEL/SILVER-COATED FOLEY CATHETER
C.R. Bard, Inc., Aug 18, 1994
K984136BARDEX LUBRI-SIL I.C. FOLEY CATHETER
Bard Medical Div., Feb 16, 1999