# FDA recall Z-2666-2026

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

## Product

1174108	PowerPICC Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741154935    1295108	PowerPICC SOLO Catheter 5 Fr Dual-Lumen  UDI-DI Code: 00801741034602    1174108D3	PowerPICC Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741154935    1174108D4	PowerPICC Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741155048    1174108D5	PowerPICC Catheter 4 Fr Singel-Lumen  UDI-DI Code: 00801741155147    1194108D	PowerPICC SOLO Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741034510    1194108D1	PowerPICC SOLO Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741154782    1194108D4	PowerPICC SOLO Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741155093    1194108D5	PowerPICC SOLO Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741155192    1275108D	PowerPICC Catheter 5 Fr Dual-Lumen  UDI-DI Code: 00801741034558    1295108FD	PowerPICC SOLO FT Catheter 5 Fr Dual-Lumen  UDI-DI Code: 00801741034626    3194108D	PowerPICC Catheter 4 Fr Single-Lumen  UDI-DI Code:  00801741027727    3275108D	PowerPICC Catheter 5 Fr Dual-Lumen  UDI-DI Code: 00801741027871    3295108D	PowerPICC SOLO FT Catheter 5 Fr Dual-Lumen  UDI-DI Code: 00801741028052    9194108D	PowerPICC SOLO Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741035609    CK000267A	PowerPICC SOLO2 Catheter  5 Fr Dual-Lumen  UDI-DI Code: 00801741185021    CK000289C	PowerPICC SOLO Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741161148    CK000293	PowerPICC HF Catheter 5 Fr Triple-Lumen  UDI-DI Code: 00801741038020    CK000586B	PowerPICC SOLO Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741212789    CK000613	PowerPICC Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741121395    CK000631B	PowerPICC Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741143748    CK000632B	PowerPICC Catheter 5 Fr Dual-Lumen  UDI-DI Code: 00801741143755    CK000746A	PowerPICC Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741227066    CK000886	PowerPICC Provena Catheter 5 Fr Triple-Lumen  UDI-DI Code: 00801741188831    CK000966A	PowerPICC Catheter 5 Fr Dual-Lumen  UDI-DI Code: 00801741215858    CK000988	PowerPICCProvena Catheter 5 Fr Triple-Lumen  UDI-DI Code: 00801741216022    CK001006	PowerPICC Provena Catheter 5 Fr Triple-Lumen  UDI-DI Code: 00801741219849    CK001030	PowerPICC SOLO Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741223976    S1275108FD2	PowerPICC Provena FT Catheter 5 Fr Dual-Lumen  UDI-Di Code: 00801741154850    S1275108FD3	PowerPICC Provena FT Catheter 5 Fr Dual-Lumen  UDI-DI Code: 00801741154959    S1295108FD1	PowerPICC Provena Catheter SOLO 5 Fr Dual-Lumen  UDI-DI Code: 00801741154805    S1295108FD3	PowerPICC Provena SOLO FT Catheter 5 Fr Dual-Lumen  UDI-DI Code: 00801741155017    S1295108FD5	PowerPICC Provena SOLO FT Catheter 5 Fr Dual-Lumen  UDI-DI Code: 00801741155215    S1385108D	PowerPICC Provena Catheter 5 Fr Triple-Lumen  UDI-DI Code: 00801741112720    S1385108D2	PowerPICC Provena Catheter 5 Fr Triple-Lumen  UDI-DI Code: 00801741154867    S1385108D3	PowerPICC Provena Catheter 5 Fr Triple-Lumen  UDI-DI Code: 00801741154966    S1385108D4	PowerPICC Provena Catheter 5 Fr Triple-Lumen  UDI-DI Code: 00801741155079    S1395108D	PowerPICC Provena SOLO Catheter 5 Fr Triple-Lumen  UDI-DI Code: 00801741112751    S1395108D1	PowerPICC Provena SOLO Catheter 5 Fr Triple-Lumen   UDI-DI Code: 00801741154812    S1395108D2	PowerPICC Provena SOLO Catheter 5 Fr Triple-Lumen  UDI-DI Code: 00801741154911    S1395108D3	PowerPICC Provena SOLO Catheter 5 Fr Triple-Lumen  UDI-DI Code: 00801741155024    S1395108D4	PowerPICC Provena SOLO Catheter 5 Fr Triple-Lumen  UDI-DI Code: 00801741155123    S1395108D5	PowerPICC Provena SOLO Catheter 5 Fr Triple-Lumen  UDI-DI Code: 00801741155222

## 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-2666-2026
- **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-2666-2026

## Citation

> MORVS. FDA recall Z-2666-2026. Retrieved 2026-10-19 from https://api.morvs.ai/recall/Z-2666-2026. Source: US FDA. Licensed CC0.

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