[Recalled] Dynesys¿ Top-Loading System Cannulated Pedicle + Set Screw — Zimmer Inc., is initiating a correction to the patient labels of products manuf… | FDA 2012-09-04
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Dynesys¿ Top-Loading System Cannulated Pedicle + Set Screw |
|---|---|
| Brand / manufacturer | Zimmer, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0242-2013 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 04 September 2012 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
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 Zimmer, 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.