# FDA recall Z-2656-2026

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

## Product

CK000495A	Poly Midline Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741121609    CK000566	Poly Midline Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741108051    CK000566	Poly Midline Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741108051      The Poly Per-Q-Cath Midline catheters are indicated for short or long term peripheral access to the peripheral venous system for selected intravenous therapies and blood sarnpling.

## 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-2656-2026
- **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-2656-2026

## Citation

> MORVS. FDA recall Z-2656-2026. Retrieved 2026-10-18 from https://api.morvs.ai/recall/Z-2656-2026. Source: US FDA. Licensed CC0.

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