Reported Jul 8, 2026 · Ongoing
CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741188770 S4153108BDP Provena Midline Catheter 3 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?
- CK000880 Provena Midline
- Catheter 4 Fr Dual-Lumen UDI-DI Code00801741188770 S4153108BDP Provena Midline
- Catheter 3 Fr Single-Lumen UDI-DI Code00801741154003 S4153108BP Provena Midline
- Catheter 3 Fr Single-Lumen UDI-DI Code00801741153990 S4153108D Provena Midline
- Catheter 3 Fr Single-Lumen UDI-DI Code00801741153952 S4153108DCP Provena Midline
- Catheter 3 Fr Single-Lumen UDI-DI Code00801741233258 S4153108DGP Provena Midline
- Catheter 3 Fr Single-Lumen UDI-DI Code00801741154027 S4254108BD Provena Midline
- Catheter 4 Fr Dual-Lumen UDI-DI Code00801741154140 S4254108BDP Provena Midline
- Catheter 4 Fr Dual-Lumen UDI-DI Code00801741154164 S4254108D Provena Midline
- Catheter 4 Fr Dual-Lumen UDI-DI Code00801741154119 S4254108DCP Provena Midline
- Catheter 4 Fr Dual-Lumen UDI-DI Code00801741233234 S4254108DGP Provena Midline
- Catheter 4 Fr Dual-Lumen UDI-DI Code00801741154188 SP4153108D Provena Midline
- Catheter 3 Fr Single-Lumen UDI-DI Code00801741185052 SP4153108DG Provena Midline
- Catheter 3 Fr Single-Lumen UDI-DI Code00801741185069 The Provena" Midline Catheters are intended for short term peripheral access for selected intravenous therapies, blood sampling, and power injection of contrast media
- Lot codes and dates
13 of 13 products
Products covered by this recall # Barcodes Product as published 1 00801741154003Lot Number: REKN2105 S4153108BDP Provena Midline Catheter 3 Fr Single-Lumen UDI-DI Code: 00801741154003 2 00801741153990Lot Numbers: REKW2429 REKX1484 S4153108BP Provena Midline Catheter 3 Fr Single-Lumen UDI-DI Code: 00801741153990 3 00801741153952Lot Number: REKW2494 S4153108D Provena Midline Catheter 3 Fr Single-Lumen UDI-DI Code: 00801741153952 4 00801741233258Lot Numbers: REKP0118 REKX2225 S4153108DCP Provena Midline Catheter 3 Fr Single-Lumen UDI-DI Code: 00801741233258 5 00801741154027Lot Number: REKX3430 S4153108DGP Provena Midline Catheter 3 Fr Single-Lumen UDI-DI Code: 00801741154027 6 00801741154140Lot Numbers: REKQ0118 REKW1477 S4254108BD Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741154140 7 00801741154164Lot Number: REKY0144 S4254108BDP Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741154164 8 00801741154119Lot Numbers: REKW0447 REKW0953 REKX2214 S4254108D Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741154119 9 00801741233234Lot Number: REKX3445 S4254108DCP Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741233234 10 00801741154188Lot Number: REKW2430 S4254108DGP Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741154188 11 00801741185052Lot Numbers: REKV3192 REKX3437 SP4153108D Provena Midline Catheter 3 Fr Single-Lumen UDI-DI Code: 00801741185052 12 00801741185069Lot Number: REKW2448 SP4153108DG Provena Midline Catheter 3 Fr Single-Lumen UDI-DI Code: 00801741185069 13 Lot Number: REKW0959 - Amount recalled
- 24,348
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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