[Recalled] Certain Gingihue Post 4.1mm(D) x 5mm(P) x 4mm(H) Item: IAPP454G Dental implants — Pouches may not have been sealed during packing | FDA 2015-11-25
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | Certain Gingihue Post 4.1mm(D) x 5mm(P) x 4mm(H) Item: IAPP454G Dental implants |
|---|---|
| Brand / manufacturer | Biomet 3i, LLC |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2413-2016 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 25 November 2015 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Pouches may not have been sealed during packing.
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 Biomet 3i, LLC
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.
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