Device recall
Z-1598-2008: Tyco Healthcare Monoject Prefill 10U/mL Heparin Lock Flush Syringe 5mL, with…
FDA device recall · Class II · Covidien LP
Key facts
| Recall number (Z-number) | Z-1598-2008 |
|---|---|
| Recall event | 47436 |
| Product | Tyco Healthcare Monoject Prefill 10U/mL Heparin Lock Flush Syringe 5mL, with BLUNTIP plastic cannula REF # 8881581125, Tyco Healthcare, Mansfield, MA 02048 |
| Product code | NZW |
| Recalling firm | Covidien LP |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 25, 2012 |
| 510(k) numbers | K032438 |
| FEI number | 1282497 |
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