Device recall
Z-2241-2010: The magnetic headrest is designed to fit the following dental chairs (THE…
FDA device recall · Class II · Dental Equipment LLC
Key facts
| Recall number (Z-number) | Z-2241-2010 |
|---|---|
| Recall event | 55153 |
| Product | The magnetic headrest is designed to fit the following dental chairs (THE HEADREST IS THE RECALLED ITEM, NOT THE CHAIRS): The dental chairs are sold under the brand names Marus and DCI Equipment. The affected models are: Marus MaxStar-Agency Model # DC1490; Marus MaxStar-Agency Model # DC1690; Marus… |
| Product code | NRU |
| Recalling firm | Dental Equipment LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 4, 2012 |
| FEI number | 1000523896 |
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