Device recall
Z-1417-2009: CHIBA NEEDLE MARKED, Model CNM-1806, Size: 18 GA x 15 CM, Qty: 10 each…
FDA device recall · Class II · Remington Medical Inc.
Key facts
| Recall number (Z-number) | Z-1417-2009 |
|---|---|
| Recall event | 51962 |
| Product | CHIBA NEEDLE MARKED, Model CNM-1806, Size: 18 GA x 15 CM, Qty: 10 each, Remington Medical, Inc., Alpharetta, GA 30005. The device is used as a General Purpose Aspiration and Injection Needle. |
| Product code | GDM |
| Recalling firm | Remington Medical Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 27, 2009 |
| FEI number | 1000132370 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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