C.R. Bard Inc recalls SureStep Foley Tray System BARD¿ Lubri-Sil Foley Catheter Tray, REF: A942216
- Recall date
- July 17, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2591-2025
- FDA classification
- Class II
- Brand / firm
- C.R. Bard Inc
- Sold / distributed
- US Nationwide distribution including in the states of NC, FL, NY, MA, MN, TX, CA, OH, MI, WA, NJ, IL, ID, SC, IN, OK, OR, AL, VA, HI, MO, MS, MD, AZ, KY, GA, IA, CO, NM, PA, ME, UT, NE.
Why it was recalled
Foley catheter trays have incorrect inserts, user may think:1)Silicone, when it's natural rubber latex, or 2)Natural rubber latex with infection control coating, when it's silicone hydrogel with antimicrobial coating, or 3)Natural latex with infection control, when it's silicone hydrogel coated without antimicrobial coating, which may cause infection and/or local and/or systemic allergic reaction
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
SureStep Foley Tray System BARD¿ Lubri-Sil Foley Catheter Tray, REF: A942216
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