Medical Device Recall: Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff Cat 60060
Bard Peripheral Vascular Inc · December 12, 2025
Reason for Recall
Due to damage to outer tray that can potentially compromise the sterile barrier
Distribution
Worldwide - U.S. Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, and WV. The countries of Argentina, Australia, Brazil, Canada, Chile, Hong Kong, India, Japan, Korea, Mexico, Malaysia, Singapore, Thailand, Uruguay, Vietnam.
States Affected
NATIONWIDE
Quantity Affected
14,935 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1367-2026
Status: ongoing
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