[Recalled] Zimmer¿ Air Dermatome II Width Plate, 2 inch. Part # 885120200. Width plate is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are plac
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | Zimmer¿ Air Dermatome II Width Plate, 2 inch. Part # 885120200. Width plate is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which is then placed into a corrugated |
|---|---|
| Brand / manufacturer | Zimmer Surgical Inc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2337-2016 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 04 July 2016 |
| EAN / barcode | 61999885 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The surface coating applied to the device is blistering, peeling and discoloring after usage over time
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 Surgical 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.