Class IIOngoingZ-2361-2026
Medartis AG recalls Medartis APTUS
The cannulation of the CCS screw is not centered.
Medartis AGJun 17, 2026
Screw, Fixation, Bone recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–6 of 6 recalls
Class IIOngoingZ-1606-2026
I.T.S. GmbH recalls HCS - Headless Compression Screw System
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
I.T.S. GmbHApr 1, 2026
Class IIOngoingZ-1599-2026
I.T.S. GmbH recalls I.T.S. Screw System with the below descriptions and corresponding article numbers.…
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
I.T.S. GmbHApr 1, 2026
Class IIOngoingZ-1550-2026
Medartis AG recalls Brand Name: APTUS Product Name: 2.8 TriLock Screw 16mm
Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws.
Medartis AGMar 18, 2026
Class IIOngoingZ-1549-2026
Medartis AG recalls Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm
Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws.
Medartis AGMar 18, 2026
Class IIOngoingZ-0957-2026
Smith & Nephew, Inc. recalls BIOSURE HA SCREW
Removal of affected lot of screws due to labeling error.
Smith & Nephew, Inc.MADec 24, 2025