Device recall
Z-1063-2010: Symbiq Pump Set, detachable, convertible pin piggyback w/backcheck valve, 3…
FDA device recall · Class II · Hospira Inc.
Key facts
| Recall number (Z-number) | Z-1063-2010 |
|---|---|
| Recall event | 54080 |
| Product | Symbiq Pump Set, detachable, convertible pin piggyback w/backcheck valve, 3 prepierced reseal ports, Option-Lok, Latex-Free, Non-DEHP, 130 in. (330 cm), 15 drops/mL; a sterile Rx single use device; Hospira Inc., Lake Forest, IL 60045 USA, Made in Costa Rica; product 196750428, list number 19675-28 |
| 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