Reported Jul 8, 2026 · Ongoing
5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen UDI-DI Code: 00801741086953 5605240…
Bard Access Systems, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.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?
- 5605150 Power-Trialysis Short-Term Straight Dialysis
- Catheter 13 Fr Triple-Lumen UDI-DI Code00801741086953 5605240 Power-Trialysis Short-Term Straight Dialysis
- Catheter 13 Fr Triple-Lumen UDI-DI Code00801741086977 5605300 Power-Trialysis Short-Term Straight Dialysis
- Catheter 13 Fr Triple-Lumen UDI-DI Code00801741086984 5615120 Power-Trialysis Short-Term Curved Extension Dialysis
- Catheter 13 Fr Triple-Lumen UDI-DI Code00801741075087 5615200 Power-Trialysis Short-Term Curved Extension Dialysis
- Catheter 13 Fr Triple-Lumen UDI-DI Code00801741075100 5615200 Power-Trialysis Short-Term Curved Extension Dialysis
- Catheter 13 Fr Triple-Lumen UDI-DI Code00801741075100 5615200 Power-Trialysis Short-Term Curved Extension Dialysis
- Catheter 13 Fr Triple-Lumen UDI-DI Code00801741075100 5655120 Power-Trialysis Short-Term Alphacurve Dialysis
- Catheter 13 Fr Triple-Lumen UDI-DI Code00801741066054 The Power-Trialysis" Short-Term Dialysis Catheter, with a third internal lumen for intravenous therapy, power injection of contrast media, and central venous pressure monitoring, is indicated for use in attaining short-term (less than 30 days) vascular access for hemodialysis, hemoperfusion, and apheresis treatments. The catheter is intended to be inserted in the jugular, femoral, or subclavian vein as required. The maximum recommended infusion rate is 5 mL/sec for power injection of contrast media
- Lot codes and dates
8 of 8 products
Products covered by this recall # Barcodes Product as published 1 00801741086977Lot Number: REKX1755 5605240 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen UDI-DI Code: 00801741086977 2 00801741086984Lot Number: REKW0663 5605300 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen UDI-DI Code: 00801741086984 3 00801741075087Lot Number: REKY2472 5615120 Power-Trialysis Short-Term Curved Extension Dialysis Catheter 13 Fr Triple-Lumen UDI-DI Code: 00801741075087 4 00801741075100Lot Number: REKZ0393 5615200 Power-Trialysis Short-Term Curved Extension Dialysis Catheter 13 Fr Triple-Lumen UDI-DI Code: 00801741075100 5 00801741075100Lot Number: REKQ1130 5615200 Power-Trialysis Short-Term Curved Extension Dialysis Catheter 13 Fr Triple-Lumen UDI-DI Code: 00801741075100 6 00801741075100Lot Number: REKX3745 5615200 Power-Trialysis Short-Term Curved Extension Dialysis Catheter 13 Fr Triple-Lumen UDI-DI Code: 00801741075100 7 00801741066054Lot Number: REKY2418 5655120 Power-Trialysis Short-Term Alphacurve Dialysis Catheter 13 Fr Triple-Lumen UDI-DI Code: 00801741066054 8 Lot Number: REKY2420 - Amount recalled
- 8,795
This recall covers 14 products
The agency filed one notice per product. You are reading one of them; the other 13 are below.
1 more are in the archive.
Where it was sold
Why it was recalled
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
This product could cause temporary or reversible health problems — stop using it.
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