Medartis recalls

Medartis has 5 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 17 Jun 2026. 4 are still ongoing. 3 were reported in the last 12 months. The most frequent reason is device malfunction.

Total recalls5since 2014

Last 12 months3reported

Class I00% of total

Ongoing4latest 17 Jun 2026

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 0 0Nov 0 0 0Feb 2 0 0May 1 0 0Aug 0 0

Severity split

Class I 0 0%Class II 5 100%Class III 0 0%

Why medartis is recalled

Product types

By year

2026360%
2024120%
2014120%

Ongoing medartis recalls

4 active

Reported	Class	Recall	Company	Reason	Where
17 Jun 2026Device	CLASS II	Aptus, 5.0 headedCCS Long Thread recalled by Medartis AG	Medartis	Other	Nationwide
18 Mar 2026Device	CLASS II	Aptus 2.8 TriLock Screw, HD7, 1/Pkg recalled by Medartis AG	Medartis	Device Malfunction	Nationwide
18 Mar 2026Device	CLASS II	Aptus 2.5 TriLock Screw, HD7, 1/Pkg recalled by Medartis AG	Medartis	Device Malfunction	Nationwide
22 May 2024Device	CLASS II	Aptus 2.8 TriLock Screw, HD7, 1/Pkg recalled by Medartis	Medartis	Foreign Material	Nationwide

All medartis recalls, newest first

5 total

Reported	Class	Recall	Company	Reason	Where
17 Jun 2026Device	CLASS II	Aptus, 5.0 headedCCS Long Thread recalled by Medartis AG	Medartis	Other	Nationwide
18 Mar 2026Device	CLASS II	Aptus 2.8 TriLock Screw, HD7, 1/Pkg recalled by Medartis AG	Medartis	Device Malfunction	Nationwide
18 Mar 2026Device	CLASS II	Aptus 2.5 TriLock Screw, HD7, 1/Pkg recalled by Medartis AG	Medartis	Device Malfunction	Nationwide
22 May 2024Device	CLASS II	Aptus 2.8 TriLock Screw, HD7, 1/Pkg recalled by Medartis	Medartis	Foreign Material	Nationwide
5 Nov 2014Device	CLASS II	Aptus Ulna Shortening recalled by Medartis	Medartis	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.