Device recall
Z-1332-2010: Lifeshield, latex-free, 150 mL Burette Set, nonvented, 117 inch with pre-pierced…
FDA device recall · Class II · Hospira Inc.
Key facts
| Recall number (Z-number) | Z-1332-2010 |
|---|---|
| Recall event | 54079 |
| Product | Lifeshield, latex-free, 150 mL Burette Set, nonvented, 117 inch with pre-pierced injection site, ball check valve, backcheck valve, 2 CLAVE ports and removable 4-way high-flow stopcock and locking spin collar, MICRODRIP, SOLUSET, 60 drops/mL, a sterile Rx single use device, Hospira Inc, Lake Forest… |
| Product code | FPA |
| Recalling firm | Hospira Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 29, 2012 |
| 510(k) numbers | K030002 |
| FEI number | 3013319212 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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