United StatesOne Step Sterile Lancet for Single Use (three sizes: 30g UDI 06949517008861 lot 2312290802; 28g UDI 06949517008854 lot 2406310201; 23g UDI 06949517008847 lot 2406310201) intended for collection of capillary blood is being recalled. Home Health US, Incorporated (Sarasota, FL) is recalling 4,661 lancets distributed nationwide through Amazon U.S. to listed states because of incorrect or missing Unique Device Identifier (UDI) codes.
What's being recalled
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.
Recalling firm: Home Health US, Incorporated, Sarasota, FL, United States.
How to identify it
UDI-DI code / Size: 06949517008861 / 30g Lot Number: 2312290802 06949517008854 / 28g Lot Number: 2406310201 06949517008847 / 23g Lot Number: 2406310201
The hazard
Due to incorrect/lack of Unique Device Identifier (UDI) codes.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
U.S.: Nation-wide distributed thru Amazon U.S. States include: AZ, CA, FL, IL, NC, NM, NY, TN, TX, and VA. O.U.S.: N/A
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)