[Recalled] Apollo Lap-Band AP System Small with RapidPort EZ Product Usage: The Lap-Band system consists of a silicone band with pillows that are filled with saline and a buckle that joins the ends of the bands together, an access port
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | Apollo Lap-Band AP System Small with RapidPort EZ Product Usage: The Lap-Band system consists of a silicone band with pillows that are filled with saline and a buckle that joins the ends of the bands together, an access port and silicone tubing that connects the band to the access port. The ban |
|---|---|
| Brand / manufacturer | Apollo Endosurgery Inc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2743-2018 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 22 November 2017 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Component of the Lap-Band system was missing from the package
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 →
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.