Bard Access Systems, Inc. recalls 5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen

Recalling company

Bard Access Systems, Inc.

Product

5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI Code: 00801741042119 The intended use of the Short-Term Dialysis Catheter is attaining temporary/short-term (less than 30 days) vascular access for hemodialysis, hemoperfusion, or apheresis therapy via the jugular, subclavian, or femoral vein.

Reason

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

Classification

Class II – may cause temporary or medically reversible health consequences

Recall date

May 21, 2026

Reported

Jul 8, 2026

Distribution

Worldwide U.S. Nationwide distribution including in the states of AK, 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, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, and WY. The country of Belgium.

Status

Ongoing

Quantity

310

Lot / codes

5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI Code: 00801741042119 Lot Number: REKY0255

Company location

Salt Lake City, UT

Recall type

Voluntary: Firm initiated

Recall number

Z-2657-2026

Agency

U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-2657-2026 in the FDA Enforcement Report. Also see FDA recall press releases.