Device recall
Z-1060-03: Medex 2000 Series Syringe Infusion Pumps. The 2001 series is a general use pump…
FDA device recall · Class II · Medex Inc
Key facts
| Recall number (Z-number) | Z-1060-03 |
|---|---|
| Recall event | 26633 |
| Product | Medex 2000 Series Syringe Infusion Pumps. The 2001 series is a general use pump, 2001E is for German use, 2001G is for use in the UK, 2001T is for use in Taiwan, 2010iK is for use in Korea (the pumps with different languages have different syringes than those used in the U.S.), 001H has a different… |
| Product code | CAJ |
| Recalling firm | Medex Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 13, 2006 |
| FEI number | 1036813 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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