Bard Access Systems DuoGlide and Power-Trialysis Short-Term Straight Dialysis Catheter
Reason given by FDA: this is a downstream recall of class I recall RES 98777.
High risk
There is a reasonable chance that using it could cause serious health problems or death.
FDA Class I recall · How risk is rated
What happened
Bard Access Systems, Inc. of Salt Lake City, Utah began a recall on August 10, 2026, of DuoGlide and Power-Trialysis Short-Term Dialysis Catheters. The FDA added the recall to its Enforcement Report on September 11, 2026, and classified it the same day. The recall was listed in the FDA's weekly enforcement report on September 23, 2026. The products were distributed across many U.S. states and the District of Columbia.
Summary by Recall Canary from the FDA notice.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Affected if its UDI-DI, lot code and reference number are listed under that product.
Power-Trialysis Short-Term Straight Dialysis Catheter
- UDI-DI
- 801741086953
- 801741086960
- 801741086977
- 801741086984
- 801741075087
- 801741075094
- 801741075100
- Reference number
- 5605150
- 5605200
- 5605240
- 5605300
- Lot
- 5605150
- REKQ2236
- REKR0948
- REKR3422
- REKR3433
- REKS1563
- REKS3564
- REKS3559
- REKT0573
- REKT1722
- REKT3057
- REKU1678
- REKV0926
- REKW0664
- REKX0410
- REKX1755
- REKY2464
- REKZ2323
- RELN2937
DuoGlide Short-Term Straight Dialysis Catheter
- UDI-DI
- 801741042096
- 801741042102
- 801741042119
- 801741042126
- 801741042133
- 801741042140
- 801741042157
- 801741042164
- 801741045714
- Reference number
- 5625150
- 5625200
- 5625240
- 5625300
- Lot
- 5625150
- REKS1082
- REKS2493
- REKU1654
- REKV2899
- REKX0416
- REKY1371
- REKZ0520
DuoGlide Short-Term Curved Extension Dialysis Catheter
- UDI-DI
- 801741042096
- 801741042102
- 801741042119
- 801741042126
- 801741042133
- 801741042140
- 801741042157
- 801741042164
- 801741045714
- Reference number
- 5626120
- 5626150
- 5626200
- 5626240
- Lot
- 5625150
- REKS1082
- REKS2493
- REKU1654
- REKV2899
- REKX0416
- REKY1371
- REKZ0520
Niagara Dual-Lumen Short-Term Curved Extension Dialysis Catheter
- UDI-DI
- 801741042096
- 801741042102
- 801741042119
- 801741042126
- 801741042133
- 801741042140
- 801741042157
- 801741042164
- 801741045714
- Reference number
- 5766200
- Lot
- 5625150
- REKS1082
- REKS2493
- REKU1654
- REKV2899
- REKX0416
- REKY1371
- REKZ0520
Power-Trialysis Short-Term Curved Extension Dialysis Catheter
- UDI-DI
- 801741086953
- 801741086960
- 801741086977
- 801741086984
- 801741075087
- 801741075094
- 801741075100
- Reference number
- 5615120
- 5615150
- 5615200
- 5615240
- Lot
- 5605150
- REKQ2236
- REKR0948
- REKR3422
- REKR3433
- REKS1563
- REKS3564
- REKS3559
- REKT0573
- REKT1722
- REKT3057
- REKU1678
- REKV0926
- REKW0664
- REKX0410
- REKX1755
- REKY2464
- REKZ2323
- RELN2937
Power-Trialysis Short-Term Alphacurve Dialysis Catheter
- UDI-DI
- 801741086953
- 801741086960
- 801741086977
- 801741086984
- 801741075087
- 801741075094
- 801741075100
- Reference number
- 5655120
- 5655150
- 5655200
- 5655240
- Lot
- 5605150
- REKQ2236
- REKR0948
- REKR3422
- REKR3433
- REKS1563
- REKS3564
- REKS3559
- REKT0573
- REKT1722
- REKT3057
- REKU1678
- REKV0926
- REKW0664
- REKX0410
- REKX1755
- REKY2464
- REKZ2323
- RELN2937
Power-Trialysis Short-Term Straight Dialysis Catheter Full Procedure Tray
- UDI-DI
- 801741086953
- 801741086960
- 801741086977
- 801741086984
- 801741075087
- 801741075094
- 801741075100
- Reference number
- 5605200G
- Lot
- 5605150
- REKQ2236
- REKR0948
- REKR3422
- REKR3433
- REKS1563
- REKS3564
- REKS3559
- REKT0573
- REKT1722
- REKT3057
- REKU1678
- REKV0926
- REKW0664
- REKX0410
- REKX1755
- REKY2464
- REKZ2323
- RELN2937
Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter
- UDI-DI
- 801741086953
- 801741086960
- 801741086977
- 801741086984
- 801741075087
- 801741075094
- 801741075100
- Reference number
- 5855200G
- 5855150
- 5855200
- 5855240
- 5855300
- Lot
- 5605150
- REKQ2236
- REKR0948
- REKR3422
- REKR3433
- REKS1563
- REKS3564
- REKS3559
- REKT0573
- REKT1722
- REKT3057
- REKU1678
- REKV0926
- REKW0664
- REKX0410
- REKX1755
- REKY2464
- REKZ2323
- RELN2937
Power-Trialysis Slim-Cath Precurved Extension Short-Term Dialysis Catheter
- UDI-DI
- 801741086953
- 801741086960
- 801741086977
- 801741086984
- 801741075087
- 801741075094
- 801741075100
- Reference number
- 5865150G
- 5865120
- 5865150
- 5865200
- 5865240
- Lot
- 5605150
- REKQ2236
- REKR0948
- REKR3422
- REKR3433
- REKS1563
- REKS3564
- REKS3559
- REKT0573
- REKT1722
- REKT3057
- REKU1678
- REKV0926
- REKW0664
- REKX0410
- REKX1755
- REKY2464
- REKZ2323
- RELN2937
Details
- Company began the recall
- Sold in
- 48 states and DC
- Alabama
- Arizona
- Arkansas
- California
- Colorado
- Connecticut
- Delaware
- District of Columbia
- Florida
- Georgia
- Hawaii
- Idaho
- Illinois
- Indiana
- Iowa
- Kansas
- Kentucky
- Louisiana
- Maine
- Maryland
- Massachusetts
- Michigan
- Minnesota
- Mississippi
- Missouri
- Montana
- Nebraska
- Nevada
- New Hampshire
- New Jersey
- New Mexico
- New York
- North Carolina
- North Dakota
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Washington
- West Virginia
- Wisconsin
- Wyoming
- Event ID
- 99534
- Recall numbers
- Z-2984-2026 to Z-2985-2026
- Company
- Bard Access Systems, Inc.Salt Lake City, Utah
- Follows FDA recall
- Spectra Medical Devices Sodium Chloride Injection (FDA 98777)
- Hazard
- Device defect
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
