[Recalled] Exactech Ambassador Cervical Plate System The Exactech Ambassador Cervical Place System is intended for anterior cervical fixation (C2-T1) for the following: degenerative disc disease (DDD) (defined as neck pain of discogenic o
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Exactech Ambassador Cervical Plate System The Exactech Ambassador Cervical Place System is intended for anterior cervical fixation (C2-T1) for the following: degenerative disc disease (DDD) (defined as neck pain of discogenic origin with degeration of the disc confirmed by history and radiographic |
|---|---|
| Brand / manufacturer | Exactech, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2070-2015 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 21 May 2015 |
| EAN / barcode | 68122001 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Shipped to a single consignee prior to completion of final inspection.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Exactech, Inc.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.