Device recall
Z-0051-2007: Kendall Monoject Syringe with Hypodermic Needle, 3cc syringe with 27 ga A-Bevel…
FDA device recall · Class II · Kendall a Division of Tyco Healthcare Group LP
Key facts
| Recall number (Z-number) | Z-0051-2007 |
|---|---|
| Recall event | 36299 |
| Product | Kendall Monoject Syringe with Hypodermic Needle, 3cc syringe with 27 ga A-Bevel Needle (3cc- 27x1-1/4 A) Product # 8881513744 |
| Product code | FMF |
| Recalling firm | Kendall a Division of Tyco Healthcare Group LP |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 11, 2009 |
| 510(k) numbers | K852544 |
| FEI number | 1317749 |
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