Linkbio Corp.: Medical Device Recall in 2023 - (Recall #: Z-1674-2023)

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:

LINK SymphoKnee System L-Shaped Femoral Augment, Medial-Right/Lateral-Left, Sz 5-6 Tilastan, cemented. Intended for primary and revision total knee replacement. Item Number: 880-325/13

Product Classification:

Class II

Date Initiated: April 25, 2023

Date Posted: June 7, 2023

Recall Number: Z-1674-2023

Event ID: 92294

Reason for Recall:

Contains the incorrect implant in the packaging. The packaging incorrectly contains the opposite side of the implant (Lateral-Right/Medial-Left instead of Medial-Right/Lateral-Left).

Status: Ongoing

Product Quantity: 11 units

Code Information:

UDI-DI : 04026575258123 Lot Number: 1910003

Distribution Pattern:

US Nationwide Distribution - AL, GA, IL, IN, LA, NV, TX

Voluntary or Mandated:

Voluntary: Firm initiated