Reported Jul 8, 2026 · Ongoing · Updated Sep 16, 2026
CK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741138478 CK000729 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?
- CK000727 PowerMidline
- Catheter 4 Fr Single-Lumen UDI-DI Code00801741138478 CK000729 PowerMidline
- Catheter 4 Fr Single-Lumen UDI-DI Code00801741138713 P4153108D PowerMidline
- Catheter 3 Fr Single-lumen UDI-DI Code00801741108747 P4154108 PowerMidline
- Catheter 4 Fr Single-Lumen UDI-DI Code00801741108754 P4154108D PowerMidline
- Catheter 4 Fr Single-Lumen UDI-DI Code00801741108761 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
5 of 5 products
Products covered by this recall # Barcodes Product as published 1 00801741138713Lot Numbers: REKP2822 REKW2840 REKX3882 CK000729 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741138713 2 00801741108747Lot Number: REKW2434 P4153108D PowerMidline Catheter 3 Fr Single-lumen UDI-DI Code: 00801741108747 3 00801741108754Lot Number: REKW0907 P4154108 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741108754 4 00801741108761Lot Numbers: REKW2479 REKX3439 P4154108D PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741108761 5 Lot Numbers: REKP0895 REKX0665 REKX2216 REKY1281 - Amount recalled
- 16,887
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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