Device recall
Z-0638-2010: Exel Huber Needles (Right angle and Straight Models with Catalog Numbers…
FDA device recall · Class I · Exelint International Co.
Key facts
| Recall number (Z-number) | Z-0638-2010 |
|---|---|
| Recall event | 54203 |
| Product | Exel Huber Needles (Right angle and Straight Models with Catalog Numbers: 26901CE, 26902CE, 26903CE, 26904CE, 26905CE, 26906CE, 26907CE, 26908CE, 26909CE, 26910CE, 26911CE, 26921CE, 26922CE, 26923CE, 26924CE, 26925CE, 26926CE, 26927CE, 26928CE, and 26929CE). |
| Product code | FMI |
| Recalling firm | Exelint International Co. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jun 6, 2011 |
| 510(k) numbers | K895769 |
| FEI number | 1035907 |
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