C.r. Bard Inc: Catheter, Retention Type, Balloon

Recall Summary C.R. Bard Inc. is recalling Silastic Brand Foley Catheters (in both 5cc and 30cc sizes) distributed across the U.S. and Canada because stains were found on the surface of some catheters. This is a Class II recall, meaning the product could cause adverse health effects but is unlikely to cause serious injury.

Recalling firm
C.R. Bard Inc
Product
Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 33420 33422 33424 Silastic Brand Foley Catheter 5cc REF: 33614 33616 33618 33620 33622 33624
Reason
Due to stain present on the surface of affected foley catheters.
Classification
Class II
Category
medical device recall
Country
United States
Agency
FDA-DEVICES
Recall date
2026-04-23
Status
Open, Classified
Areas affected
AK, AZ, AR, CA, CO, CT, FL, GA, HI, ID, IL, IN, ...
Distribution
U.S.: AK, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, and WI O.U.S.: Canada

Official recall notice from FDA-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/a252e896-fbc5-48aa-904b-3390c62ed211