Device recall
Z-1052-2010: Latex-Free Symbiq Pump Set, convertible pin, 106 inch piggyback with backcheck…
FDA device recall · Class II · Hospira Inc.
Key facts
| Recall number (Z-number) | Z-1052-2010 |
|---|---|
| Recall event | 54080 |
| Product | Latex-Free Symbiq Pump Set, convertible pin, 106 inch piggyback with backcheck valve, 2 prepierced injection sites, distal microbore tubing and OPTION-LOK, MICRODRIP, non-DEHP, 60 drops/mL; a sterile Rx device, Hospira Inc, Lake Forest, IL USA. Made in Costa Rica; product 160390428, list number… |
| Product code | FPA |
| Recalling firm | Hospira Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 29, 2012 |
| 510(k) numbers | K041550 |
| 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