Device recall
Z-2941-2026: 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235…
FDA device recall · Class II · BD SWITZERLAND SARL
Key facts
| Recall number (Z-number) | Z-2941-2026 |
|---|---|
| Recall event | 99264 |
| Product | 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 MaxPlus Ext Set w/Needleless and Y-Site REF MPX5305-C UDI-DI code: 10885403274619 9 IN Extension Set w/Max Y REF MPX5300-C UDI-DI code: 10885403237218 The Intravascular Administration Set and Extension Set is a device used… |
| Product code | FPA |
| Recalling firm | BD SWITZERLAND SARL |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K051499 |
| FEI number | 3012798826 |
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