# FDA recall Z-2659-2026

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

## Product

1274108D	PowerPICC SV Catheter 4 Fr Dual-Lumen	REKW2449	00801741087110  3173108D	PowerPICC SV Catheter 3 Fr Single-Lumen	REKV2227	00801741027536        The PowerPlCC SV catheters are intended for short or long term peripheral access to the central venous system for intravenous therapy and blood sampling.

## 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-2659-2026
- **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-2659-2026

## Citation

> MORVS. FDA recall Z-2659-2026. Retrieved 2026-10-21 from https://api.morvs.ai/recall/Z-2659-2026. Source: US FDA. Licensed CC0.

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