Basel Town, N/A, Switzerland
Medartis AG recalls
2 recalls recorded since 2018, most recently on 24 April 2026. 2 are listed as ongoing. Status and classification are as published by the FDA.
Recalls2
Ongoing (FDA)2
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 24 April 2026
- Reason
- The cannulation of the CCS screw is not centered.
- Distribution
- US Nationwide distribution in the states of LA, TX. IN, CA, NC.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2361-2026
- Medartis APTUS, 5.0 headedCCS Long Thread 50/20mm, REF A-8216.50/1, 1/Pkg; Cannulated Compression Screws for bone fixation
Ongoing Class II Medical devices
- Recall started
- 9 January 2026
- Reason
- Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws.
- Distribution
- Worldwide - US Nationwide distribution in the states of Indiana and Pennsylvania and the countries of Austria, Belgium, Switzerland, Czech Republic, Germany, Spain, Finland, France, Israel, Italy, Japan, and Poland.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-1549-2026, Z-1550-2026
- Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5750.16/1 Software Version: Not applicable. Product Description: The APTUS fixation systems are used for fractures, osteotomi
- Brand Name: APTUS Product Name: 2.8 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5850.16/1 Software Version: Not applicable. Product Description: The APTUS fixation systems are used for fractures, osteotomi
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.