LINK BIO CORP: Medical Device Recall in 2024 - (Recall #: Z-2445-2024)

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:

LINK SymphoKnee Patella Sizing Template, Item Number 881-509/00

Product Classification:

Class II

Date Initiated: June 27, 2024

Date Posted: July 31, 2024

Recall Number: Z-2445-2024

Event ID: 94926

Reason for Recall:

The LinkSymphoKnee Patella Sizing Template was incorrectly labeled. The markings on two arms of the instrument were mixed up because the triangular Patella Sizing Template was inserted upside down into the laser marking process.

Status: Ongoing

Product Quantity: 8 units

Code Information:

Item Number: 881-509/00; UDI-DI: 04026575310203; Lot number: C225066.

Distribution Pattern:

US Nationwide distribution in the states of FL, GA, KS, OH, WI.

Voluntary or Mandated:

Voluntary: Firm initiated