Reported Jul 8, 2026 · Ongoing
CK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741129674 Catheter stylets provide internal…
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?
- CK000662 PowerPICC SOLO HF
- Catheter 5 Fr Triple-Lumen UDI-DI Code00801741129674 Catheter stylets provide internal reinforcement to aid in catheter placement
- Lot codes and dates
- CK000662 PowerPICC SOLO HF
- Catheter 5 Fr Triple-Lumen UDI-DI Code00801741129674
- Lot NumberREKT1554
- Amount recalled
- 66
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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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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