FDA-Device2026-09-23Class IPACKAGING DEFECT
Bard DuoGlide Short-Term Dialysis Catheters recalled for Class I defect
What this means
Bard Access Systems is recalling multiple lots of DuoGlide Short-Term Dialysis Catheters and related models due to a Class I manufacturing defect. This is a downstream recall linked to the original Class I recall (RES 98777). The affected catheters were distributed to hospitals and dialysis centers across the U.S.
- If you manage a dialysis facility, check your inventory against the affected lot numbers and reference numbers listed in the recall notice.
- Do not use affected catheters. Contact your supplier or Bard Access Systems for instructions on returns and replacements.
- Verify the expiration dates and lot numbers on any DuoGlide catheters in stock; all listed lots expire between August 2026 and July 2027.
The agency's original wording
Hazard
this is a downstream recall of class I recall RES 98777
Intended for
Adults
Illnesses reported
None reported
Sold states
US: FL, IL, OH, VA, MD, TX, WI, GA, TN, IN, SC, NC, MI, PA, OR, OK, AZ, MS, NJ, AL, CA, CO, MA, NV, ID, MO, LA, WA, KY, IA, NH, NY, KS, HI, NE, MN, MT, WY, AR, RI, WV, UT, PR, DE, CT, ME, DC, ND, NM, SD
Affected count
22,980
Manufactured in
605 N 5600 W, N/A, Salt Lake City, UT, United States
Products
DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625150; DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625200; DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625240; DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625300; DuoGlide Short-Term Curved Extension Dialysis Catheter, REF: 5626120; DuoGlide Short-Term Curved Extension Dialysis Catheter, REF: 5626150; DuoGlide Short-Term Curved Extension Dialysis Catheter, REF: 5626200; DuoGlide Short-Term Curved Extension Dialysis Catheter, REF: 5626240; Niagara Dual-Lumen Short-Term Curved Extension Dialysis Catheter, REF: 5766200
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2985-2026More Bard recalls
- FDA-Device2026-09-23Bard Access Systems Power-Trialysis dialysis catheters recalled for potential patient harm
- FDA-Device2026-07-08Bard Access Systems Power-Trialysis dialysis catheters recalled for deficient lidocaine ampoule manufacturing
- FDA-Device2026-07-08Bard Access Systems PowerPICC catheters recalled for deficient lidocaine manufacturing
- FDA-Device2026-07-08Bard Access Systems soft tissue biopsy trays recalled for defective lidocaine ampoules
- FDA-Device2026-07-08Bard Access Systems PowerMidline Catheter recalled for deficient lidocaine ampoule manufacturing
Want us to check the next one for you?
We read every CPSC, FDA, USDA, and NHTSA notice and email you a plain-English Sunday brief covering your household — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.