# FDA recall Z-2664-2026

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

## Product

CK000525B	PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741236129    CK000883	PowerPICC Provena Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741188800    CK000884A	PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741219177    CK001000	PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741223020    CK001066	PowerPICC Provena Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741228544    CK001068	PowerPICC Provena Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741228728    S1173108D	PowerPICC Provena Catheter 3 Fr Single-Lumen  UDI-DI Code: 00801741130342    S1173108D1	PowerPICC Provena Catheter 3 Fr Single-Lumen  UDI-DI Code: 00801741154720    S1173108D4	PowerPICC Provena Catheter 3 Fr Single-Lumen   UDI-DI Code: 00801741155031    S1173108D5	PowerPICC Provena Catheter 3 Fr Single-Lumen  UDI-DI Code: 00801741155130    S1173108D6	PowerPICC Provena Catheter 3 Fr Single-Lumen  UDI-DI Code: 00801741232190    S1193108D3	PowerPICC Provena SOLO Catheter 3 Fr Single-Lumen  UDI-DI Code: 00801741154980    S1193108D4	PowerPICC Provena SOLO Catheter 3 Fr Single-Lumen  UDI-DI Code: 00801741155086    S1193108D5	PowerPICC Provena SOLO Catheter 3 Fr Single-Lumen  UDI-DI Code: 00801741155185    S1193108PD	PowerPICC Provena SOLO Catheter 3 Fr Single-Lumen  UDI-DI Code: 00801741134135    S1274108D	PowerPICC Provena  Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741130366    S1274108D4	PowerPICC Provena Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741155055    S1274108D5	PowerPICC Provena Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741155154    S1294108D	PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741130373    S1294108D2	PowerPICC Provena Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741154898    S1294108D4	PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741155109    S1294108D5	PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741155208    S3173108	PowerPICC Provena Catheter 3 Fr Single-Lumen  UDI-DI Code: 00801741130144    S3274108D	PowerPICC Provena Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741130403    S9274108D	PowerPICC Provena Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741130441      The PowerPICC Provena Catheters and PowerPICC Provena Catheter with SOLO Valve Technology are indicated for short and long term peripheral access to central venous system for intravenous therapy, blood sampling, power injection of contrast media, and allow for central venous pressure monitoring. For central venous pressure monitoring, it is recommended that a catheter lumen of 20 guage or larger be used.

## 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-2664-2026
- **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-2664-2026

## Citation

> MORVS. FDA recall Z-2664-2026. Retrieved 2026-10-20 from https://api.morvs.ai/recall/Z-2664-2026. Source: US FDA. Licensed CC0.

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