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)...
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
About Home Health US, Incorporated
Home Health US, Incorporated has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report