Device recall
Z-0056-2007: Model EMI 82691, Stic Kit Needle Containment Device. These devices are packaged…
FDA device recall · Class III · EM Innovations Inc
Key facts
| Recall number (Z-number) | Z-0056-2007 |
|---|---|
| Recall event | 36165 |
| Product | Model EMI 82691, Stic Kit Needle Containment Device. These devices are packaged 60 per case. Stick-on label on device and User Instruction sheet are attached to the case with a rubber band. |
| Product code | MMK |
| Recalling firm | EM Innovations Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Feb 21, 2007 |
| 510(k) numbers | K900035 |
| FEI number | 1000515375 |
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