Device recall
Z-1569-2011: MONOJECT Blood Collection Tubes containing heparin 13x100 sodium heparin trace…
FDA device recall · Class II · Covidien LP
Key facts
| Recall number (Z-number) | Z-1569-2011 |
|---|---|
| Recall event | 57314 |
| Product | MONOJECT Blood Collection Tubes containing heparin 13x100 sodium heparin trace element Item Code 8881307014 |
| Product code | JKA |
| Recalling firm | Covidien LP |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 4, 2015 |
| 510(k) numbers | K883320 |
| 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