FX SHOULDER: Medical Device Recall in 2024 - (Recall #: Z-0843-2024)

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:

Centered Glenosphere w/Screw, CoCr/TA6V/TiN 10-degrees Tilt 32 mm, REF: 115-3210

Product Classification:

Class II

Date Initiated: August 8, 2023

Date Posted: February 7, 2024

Recall Number: Z-0843-2024

Event ID: 93729

Reason for Recall:

Centered glenosphere box may contain an eccentric glenosphere.

Status: Ongoing

Product Quantity: 4

Code Information:

UDI-DI: 03701037309551, Lot: U0191

Distribution Pattern:

US Nationwide distribution in the state of NJ.

Voluntary or Mandated:

Voluntary: Firm initiated