Device recall
Z-0226-2026: One Step Sterile Lancet for Single Use (3 sizes): 06949517008861 30g…
FDA device recall · Class III · Home Health US, Incorporated
Key facts
| Recall number (Z-number) | Z-0226-2026 |
|---|---|
| Recall event | 97350 |
| 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… |
| Product code | QRL |
| Recalling firm | Home Health US, Incorporated |
| Recall class | Class III |
| Status | Open, Classified |
| 510(k) numbers | K222472 |
| FEI number | 3021186226 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database