Device recall
Z-1080-2010: Acacia Catalog # 385166 Dual "Y" IV Extension Set 50cm Macro Bore, Spin Nut w/BD…
FDA device recall · Class I · Medical Product Specialist Inc dba MPS Acacia
Key facts
| Recall number (Z-number) | Z-1080-2010 |
|---|---|
| Recall event | 54181 |
| Product | Acacia Catalog # 385166 Dual "Y" IV Extension Set 50cm Macro Bore, Spin Nut w/BD Q-Syte |
| Product code | FPA |
| Recalling firm | Medical Product Specialist Inc dba MPS Acacia |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jan 5, 2011 |
| 510(k) numbers | K895367 |
| FEI number | 1419937 |
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