# FDA recall Z-2667-2026

> **Bard Access Systems, Inc.** · Class II · device recall initiated 2026-05-21.

## Product

CK000880	Provena Midline Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741188770    S4153108BDP	Provena Midline Catheter 3 Fr Single-Lumen  UDI-DI Code: 00801741154003    S4153108BP	Provena Midline Catheter 3 Fr Single-Lumen  UDI-DI Code: 00801741153990    S4153108D	Provena Midline Catheter 3 Fr Single-Lumen  UDI-DI Code: 00801741153952    S4153108DCP	Provena Midline Catheter 3 Fr Single-Lumen   UDI-DI Code: 00801741233258    S4153108DGP	Provena Midline Catheter 3 Fr Single-Lumen  UDI-DI Code: 00801741154027    S4254108BD	Provena Midline Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741154140    S4254108BDP	Provena Midline Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741154164    S4254108D	Provena Midline Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741154119    S4254108DCP	Provena Midline Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741233234    S4254108DGP	Provena Midline Catheter 4 Fr Dual-Lumen   UDI-DI Code: 00801741154188    SP4153108D	Provena Midline Catheter 3 Fr Single-Lumen  UDI-DI Code: 00801741185052    SP4153108DG	Provena Midline Catheter 3 Fr Single-Lumen  UDI-DI Code: 00801741185069      The Provena" Midline Catheters are intended for short term peripheral access for selected intravenous therapies, blood sampling, and power injection of contrast media.

## Reason for recall

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

## Distribution

Worldwide U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, and WY. The country of Belgium.

## Key facts

- **Recall number:** Z-2667-2026
- **Recalling firm:** Bard Access Systems, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-05-21
- **Report date:** 2026-07-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Salt Lake City, UT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2667-2026

## Citation

> MORVS. FDA recall Z-2667-2026. Retrieved 2026-10-24 from https://api.morvs.ai/recall/Z-2667-2026. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*