Device recall
Z-2041-2009: ST ULTRAPOWER DIAMOND WHEEL (RED) 25.4mm, Catalog Number 00702109200, STERILE…
FDA device recall · Class II · Linvatec Corp. dba ConMed Linvatec
Key facts
| Recall number (Z-number) | Z-2041-2009 |
|---|---|
| Recall event | 52804 |
| Product | ST ULTRAPOWER DIAMOND WHEEL (RED) 25.4mm, Catalog Number 00702109200, STERILE, Single-use. Made is USA. ST ULTRAPOWER Diamond Wheel/MDS M-51, (MUSTARD) 25.4 mm For Use with Low or Medium Speed Drills Only, Catalog Number 00702129200, STERILE. Made in USA. ST ULTRAPOWER Diamond Wheel/MDS AM-51… |
| Product code | HTT |
| Recalling firm | Linvatec Corp. dba ConMed Linvatec |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 11, 2010 |
| FEI number | 1017294 |
At a glance
- None 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