Device recall
Z-1340-2010: Latex-free, Nitroglycerin, Midlength Secondary I.V. Pump Set, convertible pin…
FDA device recall · Class II · Hospira Inc.
Key facts
| Recall number (Z-number) | Z-1340-2010 |
|---|---|
| Recall event | 54079 |
| Product | Latex-free, Nitroglycerin, Midlength Secondary I.V. Pump Set, convertible pin, 40 inch with orange polyethylene-lined/light resistant tubing low absorption secondary set. For use only with OMNI-FLOW and PLUM series infusion systems, 15 drops/mL, a sterile Rx single use device, Hospira Inc, Lake… |
| Product code | FPA |
| Recalling firm | Hospira Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 29, 2012 |
| 510(k) numbers | K033576 |
| 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