--- title: "EBI, LLC Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search EBI, LLC recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/ebi-llc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # EBI, LLC recall records **4** reported ongoing 4 records in this archive. Latest source date Mar 22, 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 Mar 22, 2024 FDA device enforcement ### [Biomet SpinalPak Non-invasive Spine Fusion Stimulator System- Indicated for the treatment of an established nonunion acquired secondary to trauma, excluding vertebrae and all fl...](https://isitonrecall.com/recall/fda-device-z-1616-2024-biomet-spinalpak-non-invasive-spine-fusion-stimulator-system-indicated-for-the-treatment-of-an-estab/) Damage to the lead wire sheath (black cable) component and causing exposure of the wires, potentially lead to no therapeutic treatment signal being delivered to the electrodes, and result in delay of treatment Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for Biomet SpinalPak Non-invasive Spine Fusion Stimulator System- Indicated for the treatment of an e...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1616-2024%22) Mar 22, 2024 FDA device enforcement ### [Biomet OrthoPak Non-invasive Bone Growth Stimulator System-Indicated for the treatment of an established nonunion acquired secondary to trauma, excluding vertebrae and all flat ...](https://isitonrecall.com/recall/fda-device-z-1617-2024-biomet-orthopak-non-invasive-bone-growth-stimulator-system-indicated-for-the-treatment-of-an-establi/) Damage to the lead wire sheath (black cable) component and causing exposure of the wires, potentially lead to no therapeutic treatment signal being delivered to the electrodes, and result in delay of treatment Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for Biomet OrthoPak Non-invasive Bone Growth Stimulator System-Indicated for the treatment of an esta...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1617-2024%22) Mar 22, 2024 FDA device enforcement ### [20" Lead Wires, Replacement Part Number: 1067724-2](https://isitonrecall.com/recall/fda-device-z-1618-2024-20-lead-wires-replacement-part-number-1067724-2/) Damage to the lead wire sheath (black cable) component and causing exposure of the wires, potentially lead to no therapeutic treatment signal being delivered to the electrodes, and result in delay of treatment Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for 20" Lead Wires, Replacement Part Number: 1067724-2](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1618-2024%22) Mar 22, 2024 FDA device enforcement ### [48" Lead Wires, Replacement Part Number: 1067724-4](https://isitonrecall.com/recall/fda-device-z-1619-2024-48-lead-wires-replacement-part-number-1067724-4/) Damage to the lead wire sheath (black cable) component and causing exposure of the wires, potentially lead to no therapeutic treatment signal being delivered to the electrodes, and result in delay of treatment Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for 48" Lead Wires, Replacement Part Number: 1067724-4](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1619-2024%22) ## Reasons in these listed records - Damage to the lead wire sheath (black cable) component and causing exposure of the wires, potentially lead to no therapeutic treatment signal being delivered to the electrodes, and result in delay of treatment These examples come from this result page and are not a ranking of every recall reason. ## Checking EBI, LLC ### Is there a recall on ebi, llc right now? This archive contains 4 records, including 4 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 EBI, LLC](https://isitonrecall.com/check/?q=EBI%2C%20LLC) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)