Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

Curity I.V. Start Kit Recalled by Covidien LLC Due to On March 26, 2013 Covidien received a recall...

Date: April 12, 2013
Company: Covidien LLC
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 Covidien LLC directly.

Affected Products

Curity I.V. Start Kit, Product ID: 80530 and Curity I.V. Start Kit Product ID: 8508. IV Start Kit.

Quantity: 17740 kits

Why Was This Recalled?

On March 26, 2013 Covidien received a recall notice from one of their suppliers CareFusion. CareFusion is recalling a variety of OTC drug products including the 10% Povidone Iodine SEPP Applicator which is utilized in specific convenience kits.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Covidien LLC

Covidien LLC has 248 total recalls tracked by RecallDetector.

Related Recalls

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