Recall archive

94,355 stored notices, from Jun 20, 2012 to Sep 23, 2026.

3 recalls · page 1 of 1

Reported Apr 22, 2026

LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Linkbio Corp.

Matched: Brand · Product · Product details — The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 7, 2023

LINK SymphoKnee System L-Shaped Femoral Augment, Medial-Right/Lateral-Left, Sz 5-6 Tilastan, cemented. Intended for…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Linkbio Corp.

Matched: Brand — Contains the incorrect implant in the packaging. The packaging incorrectly contains the opposite side of the implant (Lateral-Right/Medial-Left…

FDA (openFDA device enforcement)

Medical devices

Reported May 10, 2023

LINK SLED Knee System: ENDO SLED KNEE FEM COMP, SMALL Item Number: 15-2020/40

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Linkbio Corp.

Matched: Brand — Additional Label Warnings: Amendment / reinforcement of the Surgical Technique and future product training on the updated technique, due to early…

47 more products in this recall

FDA (openFDA device enforcement)

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