Device recall
Z-1596-2008: Tyco Healthcare Tyco HealthcareMonoject Prefill 10U/mL Heparin Lock Flush…
FDA device recall · Class II · Covidien LP
Key facts
| Recall number (Z-number) | Z-1596-2008 |
|---|---|
| Recall event | 47436 |
| Product | Tyco Healthcare Tyco HealthcareMonoject Prefill 10U/mL Heparin Lock Flush Syringe 5mL REF # 8881580125Tyco 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