Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall 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 access port and silicone tubing that connects the band to the access port. The ban

U.S. FDA — Device Enforcement · United States · 2017-11-22 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2743-2018
Date of alert: 2017-11-22
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Apollo Endosurgery Inc
Product category: device
Product type: Devices

Reported risk: Component of the Lap-Band system was missing from the package

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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