Device recall
Z-1545-2008: Medefil Heparin I.V. Flush Syringe 1 unit/mL; a polypropylene luer locking…
FDA device recall · Class II · Medefil Incorporated
Key facts
| Recall number (Z-number) | Z-1545-2008 |
|---|---|
| Recall event | 47378 |
| Product | Medefil Heparin I.V. Flush Syringe 1 unit/mL; a polypropylene luer locking syringe containing Heparin Lock Flush Solution, USP, a sterile non-pyrogenic, isotonic injection; each mL in a Heparin I.V. Flush Syringe contains 1 unit of heparin sodium derived from porcine intestinal mucosa and 9 mg of… |
| Product code | NZW |
| Recalling firm | Medefil Incorporated |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 15, 2010 |
| FEI number | 3001677091 |
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