Device recall
Z-1496-2012: Doctors Research Group Kryptonite Bone Cement packaged in 5cc and 10 cc Kits…
FDA device recall · Class II · Doctor's Research Group, Inc.
Key facts
| Recall number (Z-number) | Z-1496-2012 |
|---|---|
| Recall event | 61709 |
| Product | Doctors Research Group Kryptonite Bone Cement packaged in 5cc and 10 cc Kits: Product Codes: KRYP-US-Z-05 (5cc Kit) KRYP-US-Z -10 (10cc Kit) Product Usage: Kryptonite Bone Cement is a resinous material indicated for use in repairing cranial defects |
| Product code | GXP |
| Recalling firm | Doctor's Research Group, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 14, 2015 |
| 510(k) numbers | K091382 |
| FEI number | 3002522629 |
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