Device recall
Z-1695-2012: Monoject Insulin Safety Syringe 3/10mL 30 X 5/16" Product ID: 8881511344…
FDA device recall · Class II · Covidien LLC
Key facts
| Recall number (Z-number) | Z-1695-2012 |
|---|---|
| Recall event | 61908 |
| Product | Monoject Insulin Safety Syringe 3/10mL 30 X 5/16" Product ID: 8881511344 Indications for Use: Injection of U-1 00 insulin |
| Product code | FMF |
| Recalling firm | Covidien LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 10, 2013 |
| 510(k) numbers | K922522 |
| FEI number | 1282497 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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