Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Apollo Lap-Band AP System Small with RapidPort EZ Product Usage: Recalled by Apollo Endosurgery Inc Due to Component of the Lap-Band system was missing from...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Apollo Endosurgery Inc directly.
Affected Products
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 band is placed laparoscopically around the stomach, creating a small pouch or stoma, thereby limiting food consumption. The band can be inflated or deflated with saline, through the access port, depending on patient needs and progress. The Lap-Band access port is a low-profile cylindrical port attached to kink-resistant tubing . The port is implanted subcutaneously or in the rectus muscle and can be penetrated in its silicone septum by a non-coring needle to inject or remove saline into or from the band. The kink-resistant tubing connects the access port to the band.
Quantity: 54
Why Was This Recalled?
Component of the Lap-Band system was missing from the package
Where Was This Sold?
This product was distributed to 11 states: FL, IL, LA, MI, MO, NY, NC, TN, TX, VA, WV
About Apollo Endosurgery Inc
Apollo Endosurgery Inc has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report