Reported Jul 8, 2026 · Ongoing
CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236150 P4254108 PowerMidline Catheter 4 Fr…
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?
- CK000980A PowerMidline
- Catheter 4 Fr Dual-Lumen UDI-DI Code00801741236150 P4254108 PowerMidline
- Catheter 4 Fr Dual-Lumen UDI-DI Code00801741129278 P4254108D PowerMidline
- Catheter 4 Fr Dual-Lumen UDI-DI Code00801741129353 The PowerMidline" Catheter is intended for short term peripheral access for selected intravenous therapies, blood sampling, and power injection of contrast media
- Lot codes and dates
3 of 3 products
Products covered by this recall # Barcodes Product as published 1 00801741129278Lot Number: REKX0112 P4254108 PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741129278 2 00801741129353Lot Number: REKW0949 P4254108D PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741129353 3 Lot Number: REJZ1337 - Amount recalled
- 2,844
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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