Technomed Europe recalls

Technomed Europe has 3 recalls on record with the FDA and USDA, the earliest in 2022 and the latest reported on 18 Sep 2024. 1 is still ongoing. The most frequent reason is sterility.

Total recalls3since 2022

Last 12 months0reported

Class I00% of total

Ongoing1latest 18 Sep 2024

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 3 100%Class III 0 0%

Why technomed europe is recalled

Sterility267%
Other Reasons133%

Product types

Syringes & Needles267%
Other Medical Devices133%

By year

2024133%
2022267%

Ongoing technomed europe recalls

1 active

Reported	Class	Recall	Company	Reason	Where
18 Sep 2024Device	CLASS II	Neurosign Disposable Stimulating Dissector recalled by Technomed Europe	Technomed Europe	Other	7 states

All technomed europe recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
18 Sep 2024Device	CLASS II	Neurosign Disposable Stimulating Dissector recalled by Technomed Europe	Technomed Europe	Other	7 states
21 Sep 2022Device	CLASS II	Disposable Subdermal Needle Electrode, Pt/lr recalled	Technomed Europe	Sterility	Nationwide
19 Jan 2022Device	CLASS II	Disposable Subdermal Needle Electrode, Corkscrew recalled	Technomed Europe	Sterility	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.