Limacorporate S.p.A: Medical Device Recall in 2023 - (Recall #: Z-2010-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

REF 1975.14.800, Prima TT Genoid Modular Reverse TT Baseplate, Sterile R

Product Classification:

Class II

Date Initiated: May 30, 2023

Date Posted: July 5, 2023

Recall Number: Z-2010-2023

Event ID: 92459

Reason for Recall:

Due to manufacturing issue, their is a potential for peripheral holes to be out of specification.

Status: Ongoing

Product Quantity: 13 units

Code Information:

UDI-DI: 08033390244893; All Lots

Distribution Pattern:

US Nationwide distribution in the states of MI, IL, ND, MO, OK.

Voluntary or Mandated:

Voluntary: Firm initiated