Device recall
Z-2816-2017: Hypodermic Needle, 23 G X 1.0 in REG BEVEL, 100 per box, 50 boxes/case…
FDA device recall · Class II · International Medsurg Connection, Inc.
Key facts
| Recall number (Z-number) | Z-2816-2017 |
|---|---|
| Recall event | 77658 |
| Product | Hypodermic Needle, 23 G X 1.0 in REG BEVEL, 100 per box, 50 boxes/case, 5,000/case The products are used to inject fluids into, or withdraw fluids from the body. They are intended for use in the diagnosis of disease or other conditions or in the cure, mitigation, treatment or prevention of disease… |
| Product code | FMI |
| Recalling firm | International Medsurg Connection, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 24, 2020 |
| 510(k) numbers | K102584 |
| FEI number | 3000210101 |
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