Device recall
Z-0830-2012: Illumena 150mL Linden Luer Syringe with Handi-Fil Straw (p/n 900103) & Illumena…
FDA device recall · Class II · Mallinckrodt Inc
Key facts
| Recall number (Z-number) | Z-0830-2012 |
|---|---|
| Recall event | 60874 |
| Product | Illumena 150mL Linden Luer Syringe with Handi-Fil Straw (p/n 900103) & Illumena 150mL Regular Luer Syringe with Handi-Fil (p/n 900101), Made in Mexico, Liebel-Flarsheim Company, Cincinnati, OH The Liebel Flarsheim Illumena 150mL Syringes with Handi-Fil Straw are designed for use with the Illumena… |
| Product code | IZQ |
| Recalling firm | Mallinckrodt Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 19, 2013 |
| 510(k) numbers | K781334 |
| FEI number | 1518293 |
At a glance
- 1–9 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