Device recall
Z-1149-2014: Heparin I.V. Flush Syringe is available is pre-filled polypropylene syringes…
FDA device recall · Class III · Medefil Incorporated
Key facts
| Recall number (Z-number) | Z-1149-2014 |
|---|---|
| Recall event | 67562 |
| Product | Heparin I.V. Flush Syringe is available is pre-filled polypropylene syringes, 100 units/mL, 3 mL fill in a 12 mL syringe. |
| Product code | NZW |
| Recalling firm | Medefil Incorporated |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 5, 2017 |
| 510(k) numbers | K092491 |
| FEI number | 3001677091 |
At a glance
- 1–9 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