Device recall
Z-0927-2007: NeatNick Sweeping Action Heel Lancet - Preemie- Item Number: 1030083 (box of…
FDA device recall · Class II · Hawaii Medical LLC
Key facts
| Recall number (Z-number) | Z-0927-2007 |
|---|---|
| Recall event | 37984 |
| Product | NeatNick Sweeping Action Heel Lancet - Preemie- Item Number: 1030083 (box of 100) and Item Number: 1030084, case of 1,000 (10 boxes of 100) |
| Product code | FMK |
| Recalling firm | Hawaii Medical LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 22, 2008 |
| FEI number | 3003827293 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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