West Lake Hills, TX, United States
Apollo Endosurgery Inc recalls
1 recall recorded since 2018, most recently on 22 November 2017. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 22 November 2017
- Terminated
- 6 October 2020
- Reason
- Component of the Lap-Band system was missing from the package
- Distribution
- Worldwide Distribution - FL, IL, LA, MI, MO, NC, NY, TN, TX, VA and WV and the countries of France, Italy, Spain, and United Kingdom
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2743-2018
- 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 ac
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.