# FDA recall Z-0226-2026

> **Home Health US, Incorporated** · Class III · device recall initiated 2025-07-25.

## Product

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.

## Reason for recall

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

## Distribution

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

## Key facts

- **Recall number:** Z-0226-2026
- **Recalling firm:** Home Health US, Incorporated
- **Classification:** Class III
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-07-25
- **Report date:** 2025-10-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Sarasota, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0226-2026

## Citation

> AI Analytics. FDA recall Z-0226-2026. Retrieved 2026-08-17 from https://api.ai-analytics.org/recall/Z-0226-2026. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*