Device recall
Z-1329-2010: Lifeshield, latex-free, 150 mL Burette Set, convertible pin, 100 inch with 2…
FDA device recall · Class II · Hospira Inc.
Key facts
| Recall number (Z-number) | Z-1329-2010 |
|---|---|
| Recall event | 54079 |
| Product | Lifeshield, latex-free, 150 mL Burette Set, convertible pin, 100 inch with 2 pre-pierced injection sites, SOLUSET, MICRODRIP, 60 drops/mL, a sterile Rx single use device, Hospira Inc, Lake Forest, IL 60045 USA. made in Costa Rica, list number 11398-20. |
| Product code | FPA |
| Recalling firm | Hospira Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 29, 2012 |
| 510(k) numbers | K941214 |
| 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