Medartis Inc.: Medical Device Recall in 2024 - (Recall #: Z-1821-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

APTUS 2.8 TriLock Screw 22mm, HD7, 1/Pkg. Metal bone fixation fastener used with the APTUS fixation system.

Product Classification:

Class II

Date Initiated: April 12, 2024

Date Posted: May 22, 2024

Recall Number: Z-1821-2024

Event ID: 94445

Reason for Recall:

Screw is 16mm long instead of 22mm long.

Status: Ongoing

Product Quantity: 110 units

Code Information:

Part No. A-5850.22/1; UDI-DI: 76300378022PA; Lot No. 24377397.

Distribution Pattern:

Worldwide - US Nationwide distribution in the state of TX and the countries of Australia, Czech Republic, Finland, France, Germany, Poland, South Africa, & Switzerland.

Voluntary or Mandated:

Voluntary: Firm initiated