--- title: "Integrity Implants Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Integrity Implants Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/integrity-implants-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Integrity Implants Inc. recall records **1** reported ongoing 5 records in this archive. Latest source date Dec 20, 2024. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Dec 20, 2024 FDA device enforcement ### [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...](https://isitonrecall.com/recall/fda-device-z-1008-2025-brand-name-n-a-product-name-repeater-bone-tamp-model-catalog-number-asy-00132-software-version-n-a-p/) Due to incompatibility of bone tamp (Rev A) and bone funnels (Rev C). Class II Reported ongoing Distribution: U.S. Nationwide distribution in the states of CA, F, GA, KY, LA, MA, MD, TN and VA. [Official source for Brand Name: N/A Product Name: Repeater Bone Tamp Model/Catalog Number: ASY-00132 Software Version...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1008-2025%22) Aug 3, 2022 FDA device enforcement ### [LineSider Spinal System pedicle screws, 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Non-cannulated. Model Number LS-N6SG6545. Thoracolumbosacral pedicle screw system; Spinal ...](https://isitonrecall.com/recall/fda-device-z-0421-2023-linesider-spinal-system-pedicle-screws-5-5-6-0mm-non-mod-standard-7-1mm-dual-lead-non-cannulated-mod/) Potential for intraoperative screw head separation at weld location. Class II Reported terminated Distribution: US distribution to California, Indiana, New York, Oklahoma, Washington DC [Official source for LineSider Spinal System pedicle screws, 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Non-cannul...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0421-2023%22) Jan 27, 2022 FDA device enforcement ### [LineSider Spinal System 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Non-cannulated. Thoracolumbosacral pedicle screw system; Spinal interlaminal fixation orthosis. Product so...](https://isitonrecall.com/recall/fda-device-z-0418-2023-linesider-spinal-system-5-5-6-0mm-non-mod-standard-7-1mm-dual-lead-non-cannulated-thoracolumbosacral/) Potential for weld separation of the Upper Tulip Head component from the Lower Tulip Head component, which would result in the separation of the Tulip Head from the Screw Shank. Class II Reported terminated Distribution: Nationwide distribution to AZ, CA, CT, DC, FL, IL, IN, LA, MA, MN, NJ, OK, PR, TN, TX, VA. [Official source for LineSider Spinal System 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Non-cannulated. Thoracolum...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0418-2023%22) Jan 27, 2022 FDA device enforcement ### [LineSider Spinal System 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Cannulated. Thoracolumbosacral pedicle screw system; Spinal interlaminal fixation orthosis. Product sold a...](https://isitonrecall.com/recall/fda-device-z-0419-2023-linesider-spinal-system-5-5-6-0mm-non-mod-standard-7-1mm-dual-lead-cannulated-thoracolumbosacral-ped/) Potential for weld separation of the Upper Tulip Head component from the Lower Tulip Head component, which would result in the separation of the Tulip Head from the Screw Shank. Class II Reported terminated Distribution: Nationwide distribution to AZ, CA, CT, DC, FL, IL, IN, LA, MA, MN, NJ, OK, PR, TN, TX, VA. [Official source for LineSider Spinal System 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Cannulated. Thoracolumbosa...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0419-2023%22) Jan 27, 2022 FDA device enforcement ### [LineSider Spinal System 5.5/6.0mm, Non-mod MIS 7.1mm - Dual Lead, Cannulated. Thoracolumbosacral pedicle screw system; Spinal interlaminal fixation orthosis. Product sold as non...](https://isitonrecall.com/recall/fda-device-z-0420-2023-linesider-spinal-system-5-5-6-0mm-non-mod-mis-7-1mm-dual-lead-cannulated-thoracolumbosacral-pedicle/) Potential for weld separation of the Upper Tulip Head component from the Lower Tulip Head component, which would result in the separation of the Tulip Head from the Screw Shank. Class II Reported terminated Distribution: Nationwide distribution to AZ, CA, CT, DC, FL, IL, IN, LA, MA, MN, NJ, OK, PR, TN, TX, VA. [Official source for LineSider Spinal System 5.5/6.0mm, Non-mod MIS 7.1mm - Dual Lead, Cannulated. Thoracolumbosacral ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0420-2023%22) ## Reasons in these listed records - Due to incompatibility of bone tamp (Rev A) and bone funnels (Rev C). - Potential for intraoperative screw head separation at weld location. - Potential for weld separation of the Upper Tulip Head component from the Lower Tulip Head component, which would result in the separation of the Tulip Head from the Screw Shank. These examples come from this result page and are not a ranking of every recall reason. ## Checking Integrity Implants Inc. ### Is there a recall on integrity implants inc. right now? This archive contains 5 records, including 1 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Integrity Implants Inc.](https://isitonrecall.com/check/?q=Integrity%20Implants%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)