--- title: "Stryker Leibinger GmbH & Co. KG Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Stryker Leibinger GmbH & Co. KG recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/stryker-leibinger-gmbh-co-kg/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Stryker Leibinger GmbH & Co. KG recall records **3** reported ongoing 4 records in this archive. Latest source date Apr 4, 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 Apr 4, 2024 FDA device enforcement ### [8000-021-002, Scopis¿ ENT Software with TGS¿ with Sofware Version: NOVA 3.6.0 RC16. Scopis is a next-generation solution for navigating functional endoscopic sinus surgery (FESS...](https://isitonrecall.com/recall/fda-device-z-1885-2024-8000-021-002-scopis-ent-software-with-tgs-with-sofware-version-nova-3-6-0-rc16-scopis-is-a-next-gene/) Unreleased software was installed on customer systems resulting in the visual feedback on the screen to show the points to be off from the physical reference point of the pointer or suction. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for 8000-021-002, Scopis¿ ENT Software with TGS¿ with Sofware Version: NOVA 3.6.0 RC16. Scopis is a n...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1885-2024%22) Mar 29, 2024 FDA device enforcement ### [Stryker 1,5/1,7MM DYNAMIC MESH- STD-MEDIUM-Intended for the reconstruction, stabilization and rigid fixation of the bony areas of the cranial skeleton. Catalog Number: 56-90614](https://isitonrecall.com/recall/fda-device-z-1785-2024-stryker-1-5-1-7mm-dynamic-mesh-std-medium-intended-for-the-reconstruction-stabilization-and-rigid-fi/) Mislabeled: Product labeled 56-90614 (90x90 Gold Mesh), was actually 56-90314 (90x90 Blue Mesh), may cause a delay in procedure Class II Reported ongoing Distribution: Nationwide [Official source for Stryker 1,5/1,7MM DYNAMIC MESH- STD-MEDIUM-Intended for the reconstruction, stabilization and rig...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1785-2024%22) Dec 6, 2022 FDA device enforcement ### [Patient-Fitted Temporomandibular (TMJ) Reconstruction Prosthesis](https://isitonrecall.com/recall/fda-device-z-1234-2023-patient-fitted-temporomandibular-tmj-reconstruction-prosthesis/) Device was shipped without having regulatory approval. Class II Reported ongoing Distribution: Distribution of one unit only to a single customer in MA (USA) [Official source for Patient-Fitted Temporomandibular (TMJ) Reconstruction Prosthesis](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1234-2023%22) Dec 29, 2021 FDA device enforcement ### [MEDPOR Titan OFW - MTB - Right - 1.0mm, Catalog number 81032](https://isitonrecall.com/recall/fda-device-z-0715-2022-medpor-titan-ofw-mtb-right-1-0mm-catalog-number-81032/) Inside the packaging of one reported item a non-conforming product was found. Contrary to the design, the barrier layer was manufactured on the inferior side of the implant versus the superior side. Class II Reported terminated Distribution: Worldwide distribution - US Nationwide. [Official source for MEDPOR Titan OFW - MTB - Right - 1.0mm, Catalog number 81032](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0715-2022%22) ## Reasons in these listed records - Unreleased software was installed on customer systems resulting in the visual feedback on the screen to show the points to be off from the physical reference point of the pointer or suction. - Mislabeled: Product labeled 56-90614 (90x90 Gold Mesh), was actually 56-90314 (90x90 Blue Mesh), may cause a delay in procedure - Device was shipped without having regulatory approval. - Inside the packaging of one reported item a non-conforming product was found. Contrary to the design, the barrier layer was manufactured on the inferior side of the implant versus the superior side. These examples come from this result page and are not a ranking of every recall reason. ## Checking Stryker Leibinger GmbH & Co. KG ### Is there a recall on stryker leibinger gmbh & co. kg right now? This archive contains 4 records, including 3 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 Stryker Leibinger GmbH & Co. KG](https://isitonrecall.com/check/?q=Stryker%20Leibinger%20GmbH%20%26%20Co.%20KG) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)