Class III — Low Risk

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

One Step Sterile Lancet for Single Use (3 sizes): 06949517008861 Recalled by Home Health US, Incorporated Due to Due to incorrect/lack of Unique Device Identifier (UDI)...

Date: July 25, 2025
Company: Home Health US, Incorporated
Status: Ongoing
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 Home Health US, Incorporated directly.

Affected Products

One Step Sterile Lancet for Single Use (3 sizes): 06949517008861 30g 06949517008854 28g 06949517008847 23g The Lancing System is intended for the hygienic collection of capillary blood for testing purposes from the side of a fingertip and from alternative sites, such as the palm, the upper arm, and the forearm.

Quantity: 4,661 lancets

Why Was This Recalled?

Due to incorrect/lack of Unique Device Identifier (UDI) codes.

Where Was This Sold?

This product was distributed to 10 states: AZ, CA, FL, IL, NM, NY, NC, TN, TX, VA

Affected (10 states)Not affected

About Home Health US, Incorporated

Home Health US, Incorporated has 1 total recall tracked by RecallDetector.

Related Recalls

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