Home Health US One Step Sterile Lancet for Single Use (3 sizes): 06949517008861 30g recall — FDA Z-0226-2026
Due to incorrect/lack of Unique Device Identifier (UDI) codes.
Overview of recall records associated with Home Health US, Inc., including dates, categories and classifications where available.
Classification mix: Class III: 1.
Due to incorrect/lack of Unique Device Identifier (UDI) codes.
This page summarizes recall records in which the official source identifies Home Health US, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.