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Integrity Implants Inc. recalls Brand Name: N/A Product Name: Repeater Bone Tamp Model/Catalog Number: ASY-00132 Software Version: N/A Product Descr
Recalled January 29, 2025 · FDA recall Z-1008-2025 · Integrity Implants
Hazard
Due to incompatibility of bone tamp (Rev A) and bone funnels (Rev C). · FDA Class II
Units
9
Sold at
U.S. Nationwide distribution in the states of CA, F, GA, KY, LA, MA, MD, TN and VA.
Description
Due to incompatibility of bone tamp (Rev A) and bone funnels (Rev C).
Product
Brand Name: N/A Product Name: Repeater Bone Tamp Model/Catalog Number: ASY-00132 Software Version: N/A Product Description: The Repeater Bone Tamp is a cylindrical shaft used to push bone graft material through a corresponding bone funnel into the FlareHawk interbody fusion device in spinal fusion procedures. Component: No
Manufacturer(s)
Integrity Implants Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →