Technomed Europe recalls
Every recall we track for Technomed Europe — 3 in all, from 2021–2024 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
3 recalls since 2017.
All FDA recall records for Technomed Europe since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 1 | 0 | 0 | 0 | 1 |
| 2022 | 0 | 1 | 0 | 0 | 1 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 1 | 0 | 1 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Technomed Europe product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Technomed Europe recalls
3 shown- Lower riskMedical device
Technomed Europe recalls NEUROSIGN Disposable Stimulating Dissector, REF 5888-00
Technomed Europe recalls NEUROSIGN Disposable Stimulating Dissector REF 5888-00 with brown discoloration on hinge area. Affected units sold with specific lot numbers. Consumers should check product for discoloration and contact for remedy.
Technomed EuropeJul 25, 2024 - Use cautionMedical device
Technomed Europe recalls Disposable Subdermal Needle Electrode, Pt/lr, 12 x 0.40mm, product number TE/S46/638, 25 needles per package, sterile.
Technomed Europe recalls disposable subdermal needle electrodes with potential MRI burns due to inadequate safety info. Affected lots expire by 2024; stop using if used in MRI.
Technomed EuropeAug 9, 2022 - Stop using nowMedical device
Technomed Europe recalls Disposable Subdermal Needle Electrode, Corkscrew, Single Use, Sterile; Model Numbers TE/S50715-001-C, TE/S50725-001C,
Technomed recalls disposable subdermal needle electrodes with a risk of blue hub detaching, leaving needles in scalp. Affected models include TE/S50715-001-C and others. Stop using immediately.
TechnomedDec 8, 2021
Technomed Europe recall questions
How many recalls has Technomed Europe had?
3 recalls from Technomed Europe are on record with U.S. safety agencies, from 2021–2024.
What is the most recent Technomed Europe recall?
Technomed Europe recalls NEUROSIGN Disposable Stimulating Dissector, REF 5888-00, dated Jul 25, 2024. Every Technomed Europe recall is listed on this page, newest first.
What should I do if I have a recalled Technomed Europe product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Technomed Europe recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.