Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LINK SymphoKnee System L-Shaped Femoral Augment Recalled by Linkbio Corp. Due to Contains the incorrect implant in the packaging. The...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Linkbio Corp. directly.
Affected Products
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
Quantity: 11 units
Why Was This Recalled?
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).
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Linkbio Corp.
Linkbio Corp. has 49 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report