Device recall
Z-1824-2012: HEPARIN LOCK FLUSH SOLUTION, USP, 10 USP Units/mL, 1 mL Multiple Dose Vial…
FDA device recall · Class II · App Pharmaceuticals Llc
Key facts
| Recall number (Z-number) | Z-1824-2012 |
|---|---|
| Recall event | 57878 |
| Product | HEPARIN LOCK FLUSH SOLUTION, USP, 10 USP Units/mL, 1 mL Multiple Dose Vial, plastic vial, vial size 3 mL, NDC 63323-544-01, Product Code 504401, Rx only To maintain patency of an indwelling venipuncture device designed for intermittent injection or infusion therapy or blood sampling. |
| Product code | NZW |
| Recalling firm | App Pharmaceuticals Llc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 20, 2012 |
| FEI number | 3002733956 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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