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Recall

Class II — C.R. Bard Inc

Recalling firmC. R. Bard, Inc.
Registered facilityView this company's 19 registered facilities → (openFDA recall records do not name a specific facility)
ClassificationClass II
StatusTerminated
ReasonThere is a potential to leak from the catheter where it connects to the drain bag
ProductBARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS14C
Quantity2120 units
DistributionUS Nationwide distribution in the states of GA, ME, NJ, WI, MN, SD, CO, ND, ID, IL, FL, LA, MD, PA, OH, NE.
Initiated2022-01-27
Classified2022-02-24
Terminated2026-07-10
Recall numberZ-0666-2022
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — C.R. Bard Inc (Z-0666-2022).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/89288/

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