Device recall
Z-0154-04: Midwest Tradition PB Non-Fiber Optic High Speed Handpiece with Push Button Chuck…
FDA device recall · Class II · DentSply -Professional Division
Key facts
| Recall number (Z-number) | Z-0154-04 |
|---|---|
| Recall event | 27578 |
| Product | Midwest Tradition PB Non-Fiber Optic High Speed Handpiece with Push Button Chuck (4 tube connection), catalog #790044; Manufactured for DENTSPLY Professional, A Division of DENTSPLY International, 901 West Oakton Street, Des plaines, IL 60018-1884 USA |
| Product code | EFB |
| Recalling firm | DentSply -Professional Division |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 3, 2004 |
| 510(k) numbers | K963050 |
| FEI number | 1419322 |
At a glance
- 1–9 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