Device recall
Z-2539-2018: AD-TECH Medical Instrument Corporation Drill Sleeve Guides DSG-6-3-090-2.4N…
FDA device recall · Class II · Ad-Tech Medical Instrument Corporation
Key facts
| Recall number (Z-number) | Z-2539-2018 |
|---|---|
| Recall event | 80280 |
| Product | AD-TECH Medical Instrument Corporation Drill Sleeve Guides DSG-6-3-090-2.4N utilizing raw material (RM0677) from the following lots from vendor 00-0001062., AD0021502, AD0021628. Product Usage: The drill sleeve guides are accessories to the Ad-Tech Cranial Drill Bits. The Cranial Drill Bits and… |
| Product code | HBE |
| Recalling firm | Ad-Tech Medical Instrument Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 8, 2019 |
| 510(k) numbers | K170442 |
| FEI number | 2183456 |
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