Device recall
Z-2798-2011: Terumo(tm) Hypodermic Needle, sterile, individually packaged into a…
FDA device recall · Class II · Terumo Medical Corporation
Key facts
| Recall number (Z-number) | Z-2798-2011 |
|---|---|
| Recall event | 58863 |
| Product | Terumo(tm) Hypodermic Needle, sterile, individually packaged into a "blister-pack" flexible plastic bottom-web thermo-formed to create a pocket, heat-sealed with paper top-web,1,000 needles per case. Product Usage: Aspiration and injection of fluids for medical purposes. |
| Product code | FMI |
| Recalling firm | Terumo Medical Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 14, 2011 |
| 510(k) numbers | K771203 |
| FEI number | 1118880 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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