Device recall
Z-0640-2010: Exel Huber Infusion Set (Catalog Numbers 26940R, 26941R, 26944R, 26945R, 26946R…
FDA device recall · Class I · Exelint International Co.
Key facts
| Recall number (Z-number) | Z-0640-2010 |
|---|---|
| Recall event | 54203 |
| Product | Exel Huber Infusion Set (Catalog Numbers 26940R, 26941R, 26944R, 26945R, 26946R, 26948R, 26949R, 26950R, 27940R, 27941R, 27944R, 27945R, 27946R, 27948R, 27949R, 27950R, 26954R, 26955R, 26958R, 26959R, 27954R, 27955R, 27958R, 27959R). |
| Product code | FPA |
| Recalling firm | Exelint International Co. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jun 6, 2011 |
| 510(k) numbers | K895770 |
| FEI number | 1035907 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ 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