Reported Sep 23, 2026 · Ongoing
Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Short-Term Straight Dialysis…
Bard Access Systems, Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Bard Access Systems, Inc. · 605 N 5600 W · Salt Lake City, UT · 84116-3738
Is this the product you have?
23 products · 169 lot codes
5605150Power-Trialysis Short-Term Straight Dialysis Catheter
- UDI-DI
801741086953
18 recalled lot codes
REKQ223608/31/2026REKR094808/31/2026REKR342209/30/2026REKR343309/30/2026REKS156310/31/2026REKS356409/30/2026REKS355910/31/2026REKT057311/30/2026REKT172209/30/2026REKT305710/31/2026REKU167812/31/2026REKV092601/31/2027REKW066402/28/2027REKX041003/31/2027REKX175503/31/2027REKY246403/31/2027REKZ232305/31/2027RELN293706/30/2027
5605200Power-Trialysis Short-Term Straight Dialysis Catheter
- UDI-DI
801741086960
20 recalled lot codes
REKQ33558/31/2026REKQ33628/31/2026REKR07569/30/2026REKR21599/30/2026REKR22149/30/2026REKS155010/31/2026REKS155910/31/2026REKS249510/31/2026REKT057610/31/2026REKT057911/30/2026REKT220111/30/2026REKT301811/30/2026REKU263612/31/2026REKU367912/31/2026REKV241512/31/2026REKW27422/28/2027REKX05763/31/2027REKX24233/31/2027REKZ05195/31/2027RELN18506/30/2027
5605240Power-Trialysis Short-Term Straight Dialysis Catheter
- UDI-DI
801741086977
11 recalled lot codes
REKQ33678/31/2026REKR07628/31/2026REKS35548/31/2026REKT217811/30/2026REKU368712/31/2026REKW06632/28/2027REKW21202/28/2027REKX056112/31/2026REKY13693/31/2027REKZ03765/31/2027RELN18356/30/2027
5605300Power-Trialysis Short-Term Straight Dialysis Catheter
- UDI-DI
801741086984
7 recalled lot codes
REKR34289/30/2026REKS248610/31/2026REKT303811/30/2026REKV167810/31/2026REKW27361/31/2027REKX37213/31/2027REKY24724/30/2027
Page 1 of 6
- Amount recalled
- 149521
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
Stop using this product now
this is a downstream recall of class I recall RES 98777
Using this product could cause serious injury, illness or death — stop using it now.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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