--- title: "Technomed Europe Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Technomed Europe recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/technomed-europe/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Technomed Europe recall records **1** reported ongoing 3 records in this archive. Latest source date Jul 25, 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 Jul 25, 2024 FDA device enforcement ### [NEUROSIGN Disposable Stimulating Dissector, REF 5888-00](https://isitonrecall.com/recall/fda-device-z-3131-2024-neurosign-disposable-stimulating-dissector-ref-5888-00/) Product has have presence of brown discoloration or substance on the hinge area of the device Class II Reported ongoing Distribution: US: FL, CA, TX, IL, NY, PA, MA [Official source for NEUROSIGN Disposable Stimulating Dissector, REF 5888-00](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3131-2024%22) Aug 9, 2022 FDA device enforcement ### [Disposable Subdermal Needle Electrode, Pt/lr, 12 x 0.40mm, product number TE/S46/638, 25 needles per package, sterile.](https://isitonrecall.com/recall/fda-device-z-1737-2022-disposable-subdermal-needle-electrode-pt-lr-12-x-0-40mm-product-number-te-s46-638-25-needles-per-pac/) Burns of varying degrees can occur to patients with electrodes left in while in the MRI scanner as a result of inadequate safety information in the IFU. Class II Reported terminated Distribution: US Nationwide distribution in the states of CA, FL, NH, OH, and WA. [Official source for Disposable Subdermal Needle Electrode, Pt/lr, 12 x 0.40mm, product number TE/S46/638, 25 needles ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1737-2022%22) Dec 8, 2021 FDA device enforcement ### [Disposable Subdermal Needle Electrode, Corkscrew, Single Use, Sterile; Model Numbers TE/S50715-001-C, TE/S50725-001C, and TE/S50715-001.](https://isitonrecall.com/recall/fda-device-z-0465-2022-disposable-subdermal-needle-electrode-corkscrew-single-use-sterile-model-numbers-te-s50715-001-c-te/) There is a high risk of the blue hub detaching from the corkscrew needle, resulting the the needle remaining in the patient's scalp. Class II Reported terminated Distribution: US Nationwide distribution in the states of California, Florida, and Ohio. [Official source for Disposable Subdermal Needle Electrode, Corkscrew, Single Use, Sterile; Model Numbers TE/S50715-00...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0465-2022%22) ## Reasons in these listed records - Product has have presence of brown discoloration or substance on the hinge area of the device - Burns of varying degrees can occur to patients with electrodes left in while in the MRI scanner as a result of inadequate safety information in the IFU. - There is a high risk of the blue hub detaching from the corkscrew needle, resulting the the needle remaining in the patient's scalp. These examples come from this result page and are not a ranking of every recall reason. ## Checking Technomed Europe ### Is there a recall on technomed europe right now? This archive contains 3 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 Technomed Europe](https://isitonrecall.com/check/?q=Technomed%20Europe) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)