Device recall
Z-0904-05: Virotek SAFEL*E*T 1.0 mm Safety Lancets, 1.0 mm depth, stock code 5000052…
FDA device recall · Class II · Efoora, Inc. dba Virotek, L.L.C.
Key facts
| Recall number (Z-number) | Z-0904-05 |
|---|---|
| Recall event | 31966 |
| Product | Virotek SAFEL*E*T 1.0 mm Safety Lancets, 1.0 mm depth, stock code 5000052, packaged in single unit blister packs, 150 or 200 per box, 6 boxes per carton; Virotek, L.L.C., 900 Asbury Dr., Buffalo Grove, IL 60089 |
| Product code | FMK |
| Recalling firm | Efoora, Inc. dba Virotek, L.L.C. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 2, 2008 |
| FEI number | 3002689104 |
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