# FDA recall Z-2662-2026

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

## Product

CK000727	PowerMidline Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741138478    CK000729	PowerMidline Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741138713    P4153108D	PowerMidline Catheter 3 Fr Single-lumen  UDI-DI Code: 00801741108747    P4154108	PowerMidline Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741108754    P4154108D	PowerMidline Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741108761      The PowerMidline" Catheter is 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-2662-2026
- **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-2662-2026

## Citation

> MORVS. FDA recall Z-2662-2026. Retrieved 2026-10-18 from https://api.morvs.ai/recall/Z-2662-2026. Source: US FDA. Licensed CC0.

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