Device recall
Z-2578-2010: ALLMED Huber Needles 22ga x.75 Straight Hub Needle - Bulk, Non-Sterile Model #…
FDA device recall · Class I · Multi-Med, Inc.
Key facts
| Recall number (Z-number) | Z-2578-2010 |
|---|---|
| Recall event | 56548 |
| Product | ALLMED Huber Needles 22ga x .75 Straight Hub Needle - Bulk, Non-Sterile Model # M2275HS-NS Reorder # 55-2235 Intended to be used to inject fluids into, withdraw fluids from inside the vascular space through a subcutaneously implanted port. |
| Product code | FMI |
| Recalling firm | Multi-Med, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jan 31, 2013 |
| 510(k) numbers | K891919 |
| FEI number | 1221765 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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