Medartis AG recalls

Medartis AG has 3 recalls on record with the FDA and USDA, the earliest in 2026 and the latest reported on 17 Jun 2026. 3 are still ongoing. 3 were reported in the last 12 months. The most frequent reason is device malfunction.

Total recalls3since 2026

Last 12 months3reported

Class I00% of total

Ongoing3latest 17 Jun 2026

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 2 0Apr 0 1 0Jul 0 0

Severity split

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

Why medartis ag is recalled

Device Malfunction267%
Other Reasons133%

Product types

Medical Software267%
Heart & Vascular Devices133%

By year

20263100%

Ongoing medartis ag recalls

3 active

Reported	Class	Recall	Company	Reason	Where
17 Jun 2026Device	CLASS II	Aptus, 0 headedCCS Long Thread recalled by Medartis AG	Medartis AG	Other	Nationwide
18 Mar 2026Device	CLASS II	Aptus 8 TriLock Screw, HD7, 1/Pkg recalled by Medartis AG	Medartis AG	Device Malfunction	Nationwide
18 Mar 2026Device	CLASS II	Aptus 5 TriLock Screw, HD7, 1/Pkg recalled by Medartis AG	Medartis AG	Device Malfunction	Nationwide

All medartis ag recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
17 Jun 2026Device	CLASS II	Aptus, 0 headedCCS Long Thread recalled by Medartis AG	Medartis AG	Other	Nationwide
18 Mar 2026Device	CLASS II	Aptus 8 TriLock Screw, HD7, 1/Pkg recalled by Medartis AG	Medartis AG	Device Malfunction	Nationwide
18 Mar 2026Device	CLASS II	Aptus 5 TriLock Screw, HD7, 1/Pkg recalled by Medartis AG	Medartis AG	Device Malfunction	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.