Technomed Europe recalls
3 official recalls and safety alerts involving Technomed Europe since 2022-01, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Technomed Europe or the relevant agency.
- 2024-09-18
USTechnomed Europe recalls NEUROSIGN Disposable Stimulating Dissector, REF 5888-00
Product has have presence of brown discoloration or substance on the hinge area of the device
- 2022-09-21
- US
Technomed Europe recalls Disposable Subdermal Needle Electrode, Pt/lr, 12 x 0.40mm, product number TE/S46/638, 25 needles per package, sterile.
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.
FDA · DeviceTechnomed EuropeUS Nationwide distribution in the states of CA, FL, NH, OH, and WA.Official notice → - 2022-01-19
- US
Technomed Europe recalls Disposable Subdermal Needle Electrode, Corkscrew, Single Use, Sterile; Model Numbers TE/S50715-001-C, TE/S50725-001C, and TE/S50715-001.
There is a high risk of the blue hub detaching from the corkscrew needle, resulting the the needle remaining in the patient's scalp.
FDA · DeviceTechnomed EuropeUS Nationwide distribution in the states of California, Florida, and Ohio.Official notice →