Device recall
Z-2161-2012: Straumann Narrow CrossFit (NC) Screw for CARES Abutment ZrO2. Endosseous dental…
FDA device recall · Class II · Straumann USA, LLC
Key facts
| Recall number (Z-number) | Z-2161-2012 |
|---|---|
| Recall event | 62575 |
| Product | Straumann Narrow CrossFit (NC) Screw for CARES Abutment ZrO2. Endosseous dental implant Article Number: 027.2650 Product Usage: Dental implants are intended for surgical placement in maxillary and/or mandibular arches to provide support for prosthetic restorations using a Straumann Narrow CrossFit… |
| Product code | NHA |
| Recalling firm | Straumann USA, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 5, 2012 |
| 510(k) numbers | K081005 |
| FEI number | 1000121052 |
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