Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
EQUISTREAM¿ XK Long-Term Hemodialysis Catheter. REF/UDI:5913230/:(01)00801741013843 Recalled by Bard Peripheral Vascular Inc Due to Incorrect Peel-Apart Introducer Sheath in Kit.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Bard Peripheral Vascular Inc directly.
Affected Products
EQUISTREAM¿ XK Long-Term Hemodialysis Catheter. REF/UDI:5913230/:(01)00801741013843; 16F
Quantity: 215
Why Was This Recalled?
Incorrect Peel-Apart Introducer Sheath in Kit.
Where Was This Sold?
This product was distributed to 24 states: AL, AZ, AR, CA, FL, GA, ID, IL, IA, KY, LA, MD, MN, MT, NY, NC, OR, PA, TN, TX, VA, WA, WV, WI
About Bard Peripheral Vascular Inc
Bard Peripheral Vascular Inc has 136 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report