Class II — Potential Health Hazard

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

5.5 Fr x 40 cm double-lumen PICC Kit Recalled by Arrow International Inc Due to The products may contain the incorrect catheter. Kits...

Date: July 17, 2018
Company: Arrow International 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 Arrow International Inc directly.

Affected Products

5.5 Fr x 40 cm double-lumen PICC Kit, Product Code CDC-44052-VPS2

Quantity: 1257 total

Why Was This Recalled?

The products may contain the incorrect catheter. Kits that should contain a 4.5 Fr single-lumen catheter may contain a 5.5 Fr double-lumen catheter. Kits that should contain a 5.5 Fr double-lumen catheter may contain a 4.5 Fr single-lumen catheter. This issue may cause a delay in treatment while a replacement catheter is obtained.

Where Was This Sold?

This product was distributed to 14 states: AL, AZ, CA, GA, ME, MD, MA, MI, NY, PA, RI, SC, VA, WA

Affected (14 states)Not affected

About Arrow International Inc

Arrow International Inc has 431 total recalls tracked by RecallDetector.

Related Recalls

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