Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

5Fr PowerPICC Catheter Single-Lumen with 70cm Guidewire Instructions For Use: Recalled by Bard Access Systems Inc. Due to Catheter kits contained the incorrect micro-introducers.

Date: May 19, 2021
Company: Bard Access Systems Inc.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Bard Access Systems Inc. directly.

Affected Products

5Fr PowerPICC Catheter Single-Lumen with 70cm Guidewire Instructions For Use: PowerPicc Polyurethand Radiology PiCC with Microintroducer

Quantity: 180 units

Why Was This Recalled?

Catheter kits contained the incorrect micro-introducers.

Where Was This Sold?

This product was distributed to 10 states: CT, GA, MA, MI, MT, NV, NJ, NY, VA, WI

Affected (10 states)Not affected

About Bard Access Systems Inc.

Bard Access Systems Inc. has 22 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report