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Linkbio Corp. recalls LINK SymphoKnee System L-Shaped Femoral Augment, Medial-Right/Lateral-Left, Sz 5-6 Tilastan, cemented. Intended for pr
Recalled June 7, 2023 · FDA recall Z-1674-2023 · Linkbio
Hazard
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). · FDA Class II
Units
11 units
Sold at
US Nationwide Distribution - AL, GA, IL, IN, LA, NV, TX
Description
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).
Product
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
Manufacturer(s)
Linkbio Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →